Visible‐Light Photoredox‐Catalyzed Hydrodecarboxylation and Deuterodecarboxylation of Fatty Acids

Comprehensive Summary We develop an efficient visible‐light photoreodox‐catalyzed hydrodecarboxylation and deuterodecarboxylation of fatty acids for alkanes and deuterium alkanes. The key to the efficient transformation should attribute to the co‐catalysis of the suitable methoxy substituted acridin...

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Published inChinese journal of chemistry Vol. 40; no. 16; pp. 1903 - 1908
Main Authors Sun, Yuan‐Li, Tan, Fang‐Fang, Hu, Rong‐Gui, Hu, Chun‐Hong, Li, Yang
Format Journal Article
LanguageEnglish
Published Weinheim WILEY‐VCH Verlag GmbH & Co. KGaA 15.08.2022
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Abstract Comprehensive Summary We develop an efficient visible‐light photoreodox‐catalyzed hydrodecarboxylation and deuterodecarboxylation of fatty acids for alkanes and deuterium alkanes. The key to the efficient transformation should attribute to the co‐catalysis of the suitable methoxy substituted acridine photocatalyst (Mes‐1,3,6,8‐tetramethoxy‐Acr‐3”,5”‐dimethoxy‐Ph) and the hydrogen atom transfer catalyst 4′,4′‐dimethyl diphenyldisulfane, possibly via facilitating of quenching the active alkyl radicals to overcome the competitive homocoupling products, olefins via the disproportionation, cracking products via the C—C bond β‐scission. Highly efficient hydrodecarboxylation and deuterodecarboxylation of fatty acids for alkanes and deuterium alkanes are developed, by co‐catalysis of the methoxy substituted acridine photocatalyst and the HAT catalyst under visible‐light irradiation.
AbstractList Comprehensive Summary We develop an efficient visible‐light photoreodox‐catalyzed hydrodecarboxylation and deuterodecarboxylation of fatty acids for alkanes and deuterium alkanes. The key to the efficient transformation should attribute to the co‐catalysis of the suitable methoxy substituted acridine photocatalyst (Mes‐1,3,6,8‐tetramethoxy‐Acr‐3”,5”‐dimethoxy‐Ph) and the hydrogen atom transfer catalyst 4′,4′‐dimethyl diphenyldisulfane, possibly via facilitating of quenching the active alkyl radicals to overcome the competitive homocoupling products, olefins via the disproportionation, cracking products via the C—C bond β‐scission.
Comprehensive Summary We develop an efficient visible‐light photoreodox‐catalyzed hydrodecarboxylation and deuterodecarboxylation of fatty acids for alkanes and deuterium alkanes. The key to the efficient transformation should attribute to the co‐catalysis of the suitable methoxy substituted acridine photocatalyst (Mes‐1,3,6,8‐tetramethoxy‐Acr‐3”,5”‐dimethoxy‐Ph) and the hydrogen atom transfer catalyst 4′,4′‐dimethyl diphenyldisulfane, possibly via facilitating of quenching the active alkyl radicals to overcome the competitive homocoupling products, olefins via the disproportionation, cracking products via the C—C bond β‐scission. Highly efficient hydrodecarboxylation and deuterodecarboxylation of fatty acids for alkanes and deuterium alkanes are developed, by co‐catalysis of the methoxy substituted acridine photocatalyst and the HAT catalyst under visible‐light irradiation.
Comprehensive SummaryWe develop an efficient visible‐light photoreodox‐catalyzed hydrodecarboxylation and deuterodecarboxylation of fatty acids for alkanes and deuterium alkanes. The key to the efficient transformation should attribute to the co‐catalysis of the suitable methoxy substituted acridine photocatalyst (Mes‐1,3,6,8‐tetramethoxy‐Acr‐3”,5”‐dimethoxy‐Ph) and the hydrogen atom transfer catalyst 4′,4′‐dimethyl diphenyldisulfane, possibly via facilitating of quenching the active alkyl radicals to overcome the competitive homocoupling products, olefins via the disproportionation, cracking products via the C—C bond β‐scission.
Author Hu, Rong‐Gui
Tan, Fang‐Fang
Li, Yang
Sun, Yuan‐Li
Hu, Chun‐Hong
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  organization: Center for Organic Chemistry, Frontier Institute of Science and Technology, Xi'an Jiaotong University, Xi'an
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Cites_doi 10.1002/cssc.200900107
10.1002/anie.201704146
10.1021/acscatal.6b00520
10.1021/ja306168h
10.1002/cssc.201300370
10.1021/j100342a049
10.1126/science.1159210
10.1016/j.jclepro.2016.12.163
10.1002/anie.201904671
10.3390/catal11091118
10.1021/i100009a023
10.1038/nchem.2000
10.1021/ja000112q
10.1021/acssuschemeng.8b04488
10.1021/jacs.1c07562
10.1021/jacs.1c05852
10.1002/chem.201905224
10.1021/cr300503r
10.1039/a804291h
10.1021/acs.iecr.0c02187
10.1021/acs.chemrev.6b00018
10.1039/C8SE00189H
10.1039/D0GC02901G
10.1021/acs.accounts.6b00229
10.1021/ol5019294
10.1038/s41586-020-2131-1
10.1021/ar400200u
10.1002/anie.201709523
10.1021/acs.accounts.6b00270
10.1038/s41467-021-24259-6
10.1021/jacs.5b07770
10.1021/ie400790v
10.1021/ja506228u
10.1039/C8GC03745K
10.1126/science.1111166
10.1021/jm4007998
10.1021/ja038656q
10.1016/j.scib.2020.03.017
10.1021/ol200290m
10.1021/ja003811b
10.1038/s41929-020-0423-3
10.1016/S0040-4039(01)00370-7
10.1039/C5CS00859J
10.1021/acs.chemrev.6b00057
10.1039/D1SC00528F
10.1021/acs.jpca.6b11472
10.1039/c0cc01464h
10.1038/s41467-020-19944-x
10.1021/ol502625w
10.1039/b714526h
10.1002/anie.201711296
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References 2017 2014; 56 6
2001; 123
2018 2019; 6 21
2013 2005; 52 308
2018 2018 2020; 57 29 11
2011 2020; 13 26
2015; 137
1998 2021 2021; 28 143 143
2008 2020 2009 2013 2016 2017 2021; 322 3 2 6 45 143 11
1682 2007; 1971
2014 2020; 136 580
2017 2018; 121 2
2014; 57
2019 2021 2021; 58 12 12
2014 2014 2020; 16 16 65
2004
2016 2016 2016 2016; 49 49 116 116
2000; 122
2020; 22
2004 2014; 126 47
1988; 93
2016 2020; 6 59
1983; 22
2001; 42
e_1_2_6_19_1
Davidson R. S. (e_1_2_6_9_1) 1682; 1971
e_1_2_6_13_1
e_1_2_6_15_3
e_1_2_6_17_1
e_1_2_6_15_4
e_1_2_6_17_2
e_1_2_6_15_1
e_1_2_6_15_2
e_1_2_6_20_2
e_1_2_6_20_1
Sparr C. (e_1_2_6_18_2) 2018; 29
e_1_2_6_3_7
e_1_2_6_5_5
e_1_2_6_7_3
e_1_2_6_3_6
e_1_2_6_5_4
e_1_2_6_7_2
e_1_2_6_9_2
e_1_2_6_3_3
e_1_2_6_5_1
e_1_2_6_3_2
e_1_2_6_3_5
e_1_2_6_5_3
e_1_2_6_7_1
e_1_2_6_3_4
e_1_2_6_5_2
e_1_2_6_22_3
e_1_2_6_24_1
e_1_2_6_3_1
e_1_2_6_22_2
e_1_2_6_22_1
e_1_2_6_10_1
e_1_2_6_18_3
e_1_2_6_12_2
e_1_2_6_14_1
e_1_2_6_12_1
e_1_2_6_16_2
e_1_2_6_18_1
e_1_2_6_16_1
e_1_2_6_21_1
e_1_2_6_6_4
e_1_2_6_8_2
e_1_2_6_6_3
e_1_2_6_8_1
Bégué J.‐P. (e_1_2_6_11_1) 2004
e_1_2_6_8_3
e_1_2_6_4_2
e_1_2_6_4_1
e_1_2_6_6_2
e_1_2_6_6_1
e_1_2_6_25_1
e_1_2_6_23_2
e_1_2_6_2_2
e_1_2_6_23_1
e_1_2_6_2_1
References_xml – volume: 16 16 65
  start-page: 4228 5394 870
  year: 2014 2014 2020
  end-page: 4231 5397 871
  article-title: Photocatalytic Decarboxylative Reduction of Carboxylic Acids and Its Application in Asymmetric Synthesis A Clean and Selective Radical Homocoupling Employing Carboxylic Acids with Titania Photoredox Catalysis Photocatalytic Alkane Production from Fatty Acid Decarboxylation over Hydrogenated Catalyst
  publication-title: Org. Lett. Org. Lett. Sci. Bull.
– volume: 136 580
  start-page: 17024 76
  year: 2014 2020
  end-page: 17035 80
  article-title: Mechanistic Insight into the Photoredox Catalysis of Anti‐Markovnikov Alkene Hydrofunctionalization Reactions Discovery and Characterization of an Acridine Radical Photoreductant
  publication-title: J. Am. Chem. Soc. Nature
– volume: 123
  start-page: 1723
  year: 2001
  end-page: 1729
  article-title: Substituent Effects on the Oxidation and Reduction Potentials of Phenylthiyl Radicals in Acetonitrile
  publication-title: J. Am. Chem. Soc.
– volume: 122
  start-page: 7953
  year: 2000
  end-page: 7975
  article-title: Inter‐ and Intramolecular Experimental and Calculated Equilibrium Isotope Effects for (silox) ( Bu SiND)TiR + RH (silox = Bu SiO): Inferred Kinetic Isotope Effects for RH/D Addition to Transient (silox) Ti=NSi Bu
  publication-title: J. Am. Chem. Soc.
– volume: 56 6
  start-page: 15644 720
  year: 2017 2014
  end-page: 15648 726
  article-title: Direct Aryl C‐H Amination with Primary Amines Using Organic Photoredox Catalysis The Direct Anti‐Markovnikov Addition of Mineral Acids to Styrenes
  publication-title: Angew. Chem. Int. Ed. Nat. Chem.
– volume: 1971
  start-page: 5244
  year: 1682 2007
  end-page: 5246
  article-title: The Photosensitized Decarboxylation of Carboxylic Acids by Benzophenone and Quinones Decarboxylative Reduction of Free Aliphatic Carboxylic Acids by Photogenerated Cation Radical
  publication-title: J. Chem. Soc. C Chem. Commun.
– start-page: 18
  year: 2004
  end-page: 29
  article-title: Fluorinated Alcohols: A New Medium for Selective and Clean Reaction
  publication-title: Synlett
– volume: 28 143 143
  start-page: 25 11251 13022
  year: 1998 2021 2021
  end-page: 35 11261 13028
  article-title: Polarity‐reversal catalysis of hydrogen‐atom abstraction reactions: concepts and applications in organic chemistry Hydroalkylation of Unactivated Olefins via Visible‐Light‐Driven Dual Hydrogen Atom Transfer Catalysis Photoinduced Hydrocarboxylation via Thiol‐Catalyzed Delivery of Formate Across Activated Alkenes
  publication-title: Chem. Soc. Rev. J. Am. Chem. Soc. J. Am. Chem. Soc.
– volume: 6 59
  start-page: 4512 17440
  year: 2016 2020
  end-page: 4525 17450
  article-title: Development of a Bimetallic Pd‐Ni/HZSM‐5 Catalyst for the Tandem Limonene Dehydrogenation and Fatty Acid Deoxygenation to Alkanes and Arenes for Use as Biojet Fuel Catalytic Hydrodeoxygenation of Methyl Stearate and Microbial Lipids to Diesel‐Range Alkanes over Pd/HPA‐SiO Catalysts
  publication-title: ACS Catal. Ind. Eng. Chem. Res.
– volume: 6 21
  start-page: 17108 2334
  year: 2018 2019
  end-page: 17113 2344
  article-title: Producing Widespread Monomers from Biomass Using Economical Carbon and Ruthenium–Titanium Dioxide Electrocatalysts Electrochemical Cross‐Coupling of Biogenic Diacids for Sustainable Fuel Production
  publication-title: ACS Sustainable Chem. Eng. Green Chem.
– volume: 42
  start-page: 3137
  year: 2001
  end-page: 3140
  article-title: Radical Cyclisation Reactions Involving Phosphonyl Radicals: The Use of Phosphites and Phosphine Oxides as Alternatives to Tributyltin Hydride
  publication-title: Tetrahedron Lett.
– volume: 126 47
  start-page: 1600 1455
  year: 2004 2014
  end-page: 1601 1464
  article-title: Electron‐Transfer State of 9‐Mesityl‐10‐methylacridinium Ion with a Much Longer Lifetime and Higher Energy Than That of the Natural Photosynthetic Reaction Center Long‐Lived Charge Separation and Applications in Artificial Photosynthesis
  publication-title: J. Am. Chem. Soc. Acc. Chem. Res.
– volume: 121 2
  start-page: 1261 1837
  year: 2017 2018
  end-page: 1280 1843
  article-title: Catalytic Decarbonylation of Stearic Acid to Hydrocarbons over Activated Carbon‐Supported Nickel
  publication-title: J. Phys. Chem. A Sustain. Energy Fuels
– volume: 137
  start-page: 11340
  year: 2015
  end-page: 11348
  article-title: Hydrodecarboxylation of Carboxylic and Malonic Acid Derivatives via Organic Photoredox Catalysis: Substrate Scope and Mechanistic Insight
  publication-title: J. Am. Chem. Soc.
– volume: 57 29 11
  start-page: 2436 2176 6126
  year: 2018 2018 2020
  end-page: 2440 2180
  article-title: Direct Transformation of Esters into Heterocyclic Fluorophores Visible‐Light Photoredox‐Catalyzed C‐O Bond Cleavage of Diaryl Ethers by Acridinium Photocatalysts at Room Temperature
  publication-title: Angew. Chem. Int. Ed. Configurationally Stable Atropisomeric Acridinium Fluorophores. Synlett Nat. Commun.
– volume: 57
  start-page: 3595
  year: 2014
  end-page: 3611
  article-title: Using Deuterium in Drug Discovery: Leaving the Label in the Drug
  publication-title: J. Med. Chem.
– volume: 22
  start-page: 132
  year: 1983
  end-page: 139
  article-title: Initial Product Distributions from Pyrolysis of Normal and Branched Paraffins
  publication-title: Ind. Eng. Chem. Fundam.
– volume: 322 3 2 6 45 143 11
  start-page: 417 170 1109 1576 584 1 1118
  year: 2008 2020 2009 2013 2016 2017 2021
  end-page: 421 178 1119 1594 611 9 1157
  article-title: Catalytic Conversion of Biomass to Monofunctional Hydrocarbons and Targeted Liquid‐Fuel Classes Enhanced Photocatalytic Alkane Production from Fatty Acid Decarboxylation via Inhibition of Radical Oligomerization Transforming Triglycerides and Fatty Acids into Biofuels Reaction Pathways for the Deoxygenation of Vegetable Oils and Related Model Compounds Potential and challenges of zeolite chemistry in the catalytic conversion of biomass Palm Fatty Acid Distillate as a Potential Source for Biodiesel Production‐A Review The Catalysed Transformation of Vegetable Oils or Animal Fats to Biofuels and Bio‐Lubricants: A Review
  publication-title: Science Nat. Catal. ChemSusChem ChemSusChem Chem. Soc. Rev. J. Clean. Prod. Catalysts
– volume: 58 12 12
  start-page: 10514 5505 3983
  year: 2019 2021 2021
  end-page: 10520 5510
  article-title: Visible‐Light‐Photosensitized Aryl and Alkyl Decarboxylative Functionalization Reactions A Highly Selective Decarboxylative Deuteration of Carboxylic Acids Light‐Driven Decarboxylative Deuteration Enabled by a Divergently Engineered Photodecarboxylase
  publication-title: Angew. Chem. Int. Ed. Chem. Sci. Nat. Commun.
– volume: 13 26
  start-page: 1944 3226
  year: 2011 2020
  end-page: 1947 3230
  article-title: Reducing the Cost, Smell, and Toxicity of the Barton Reductive Decarboxylation: Chloroform as the Hydrogen Atom Source Catalyst‐Free Decarboxylation of Carboxylic Acids and Deoxygenation of Alcohols by Electro‐Induced Radical Formation
  publication-title: Org. Lett. Chem. ‐ Eur. J.
– volume: 52 308
  start-page: 10114 1446
  year: 2013 2005
  end-page: 10125 1450
  article-title: Value Added Hydrocarbons from Distilled Tall Oil via Hydrotreating over a Commercial NiMo Catalyst Production of Liquid Alkanes by Aqueous‐Phase Processing of Biomass‐Derived Carbohydrates
  publication-title: Ind. Eng. Chem. Res. Science
– volume: 22
  start-page: 7725
  year: 2020
  end-page: 7736
  article-title: Photochemical Methods for Deuterium Labelling of Organic Molecules
  publication-title: Green Chem.
– volume: 93
  start-page: 1944
  year: 1988
  end-page: 1947
  article-title: Hydrogen‐Atom Abstraction from Methanol by OH
  publication-title: J. Phys. Chem.
– volume: 49 49 116 116
  start-page: 1566 2295 10035 10075
  year: 2016 2016 2016 2016
  end-page: 1577 2306 10074 10166
  article-title: Visible Light Mediated Photoredox Catalytic Arylation Reactions Free Radical Chemistry Enabled by Visible Light‐Induced Electron Transfer Dual Catalysis Strategies in Photochemical Synthesis
  publication-title: Acc. Chem. Res. Acc. Chem. Res. Chem. Rev. Organic Photoredox Catalysis. Chem. Rev.
– ident: e_1_2_6_3_3
  doi: 10.1002/cssc.200900107
– ident: e_1_2_6_12_1
  doi: 10.1002/anie.201704146
– ident: e_1_2_6_4_1
  doi: 10.1021/acscatal.6b00520
– ident: e_1_2_6_6_1
  doi: 10.1021/ja306168h
– ident: e_1_2_6_3_4
  doi: 10.1002/cssc.201300370
– ident: e_1_2_6_19_1
  doi: 10.1021/j100342a049
– ident: e_1_2_6_3_1
  doi: 10.1126/science.1159210
– ident: e_1_2_6_3_6
  doi: 10.1016/j.jclepro.2016.12.163
– ident: e_1_2_6_15_2
  doi: 10.1002/anie.201904671
– ident: e_1_2_6_3_7
  doi: 10.3390/catal11091118
– ident: e_1_2_6_24_1
  doi: 10.1021/i100009a023
– ident: e_1_2_6_20_2
  doi: 10.1038/nchem.2000
– ident: e_1_2_6_13_1
  doi: 10.1021/ja000112q
– ident: e_1_2_6_7_2
  doi: 10.1021/acssuschemeng.8b04488
– ident: e_1_2_6_22_3
  doi: 10.1021/jacs.1c07562
– ident: e_1_2_6_22_2
  doi: 10.1021/jacs.1c05852
– ident: e_1_2_6_23_2
  doi: 10.1002/chem.201905224
– ident: e_1_2_6_5_1
  doi: 10.1021/cr300503r
– ident: e_1_2_6_22_1
  doi: 10.1039/a804291h
– ident: e_1_2_6_4_2
  doi: 10.1021/acs.iecr.0c02187
– ident: e_1_2_6_8_3
– ident: e_1_2_6_5_4
  doi: 10.1021/acs.chemrev.6b00018
– ident: e_1_2_6_8_2
  doi: 10.1039/C8SE00189H
– ident: e_1_2_6_14_1
  doi: 10.1039/D0GC02901G
– ident: e_1_2_6_5_2
  doi: 10.1021/acs.accounts.6b00229
– ident: e_1_2_6_6_2
  doi: 10.1021/ol5019294
– ident: e_1_2_6_17_2
  doi: 10.1038/s41586-020-2131-1
– ident: e_1_2_6_16_2
  doi: 10.1021/ar400200u
– ident: e_1_2_6_20_1
  doi: 10.1002/anie.201709523
– ident: e_1_2_6_5_3
  doi: 10.1021/acs.accounts.6b00270
– ident: e_1_2_6_15_4
  doi: 10.1038/s41467-021-24259-6
– ident: e_1_2_6_10_1
  doi: 10.1021/jacs.5b07770
– ident: e_1_2_6_2_1
  doi: 10.1021/ie400790v
– ident: e_1_2_6_17_1
  doi: 10.1021/ja506228u
– ident: e_1_2_6_7_3
  doi: 10.1039/C8GC03745K
– ident: e_1_2_6_2_2
  doi: 10.1126/science.1111166
– ident: e_1_2_6_7_1
– ident: e_1_2_6_12_2
  doi: 10.1021/jm4007998
– ident: e_1_2_6_16_1
  doi: 10.1021/ja038656q
– ident: e_1_2_6_6_4
  doi: 10.1016/j.scib.2020.03.017
– ident: e_1_2_6_23_1
  doi: 10.1021/ol200290m
– ident: e_1_2_6_21_1
  doi: 10.1021/ja003811b
– volume: 1971
  year: 1682
  ident: e_1_2_6_9_1
  article-title: The Photosensitized Decarboxylation of Carboxylic Acids by Benzophenone and Quinones
  publication-title: J. Chem. Soc. C
  contributor:
    fullname: Davidson R. S.
– ident: e_1_2_6_3_2
  doi: 10.1038/s41929-020-0423-3
– ident: e_1_2_6_25_1
  doi: 10.1016/S0040-4039(01)00370-7
– ident: e_1_2_6_3_5
  doi: 10.1039/C5CS00859J
– ident: e_1_2_6_5_5
  doi: 10.1021/acs.chemrev.6b00057
– ident: e_1_2_6_15_3
  doi: 10.1039/D1SC00528F
– ident: e_1_2_6_8_1
  doi: 10.1021/acs.jpca.6b11472
– ident: e_1_2_6_15_1
  doi: 10.1039/c0cc01464h
– start-page: 18
  year: 2004
  ident: e_1_2_6_11_1
  article-title: Fluorinated Alcohols: A New Medium for Selective and Clean Reaction
  publication-title: Synlett
  contributor:
    fullname: Bégué J.‐P.
– ident: e_1_2_6_18_3
  doi: 10.1038/s41467-020-19944-x
– volume: 29
  start-page: 2176
  year: 2018
  ident: e_1_2_6_18_2
  publication-title: Configurationally Stable Atropisomeric Acridinium Fluorophores. Synlett
  contributor:
    fullname: Sparr C.
– ident: e_1_2_6_6_3
  doi: 10.1021/ol502625w
– ident: e_1_2_6_9_2
  doi: 10.1039/b714526h
– ident: e_1_2_6_18_1
  doi: 10.1002/anie.201711296
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Snippet Comprehensive Summary We develop an efficient visible‐light photoreodox‐catalyzed hydrodecarboxylation and deuterodecarboxylation of fatty acids for alkanes...
Comprehensive SummaryWe develop an efficient visible‐light photoreodox‐catalyzed hydrodecarboxylation and deuterodecarboxylation of fatty acids for alkanes and...
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wiley
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StartPage 1903
SubjectTerms Alkanes
Alkenes
Catalysis
Catalysts
Cleavage
Deuterium
Deuterodecarboxylation
Disproportionation
Fatty acids
Hydrodecarboxylation
Hydrogen atoms
Photocatalysis
Title Visible‐Light Photoredox‐Catalyzed Hydrodecarboxylation and Deuterodecarboxylation of Fatty Acids
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