Synthesis of terminally perfluorinated long-chain alkanethiols, sulfides and disulfides from the corresponding halides

• Published in: Journal of fluorine chemistry Vol. 104; no. 2; pp. 173 - 183
• Main Authors: Naud, C, Calas, P, Blancou, H, Commeyras, A
• Format: Journal Article
• Language: English
• Published: LAUSANNE Elsevier B.V 01.07.2000; Elsevier
• Subjects: Chemistry; Chemistry, Inorganic & Nuclear; Chemistry, Organic; Disulfides; Physical Sciences; Science & Technology; Sulfides; Terminally perfluorinated long — chain alkanethiols; Sulfides; Terminally perfluorinated long — chain alkanethiols; Disulfides; disulfides; IODIDES; terminally perfluorinated long - chain alkanethiols; sulfides
• ISSN: 0022-1139; 1873-3328
• DOI: 10.1016/S0022-1139(00)00215-3

Semifluorinated n-alkanethiols, symmetrical sulfides and disulfides bearing the chain(s) F(CF 2) n (CH 2) m with n=4, 6, 8, 10, and m=2, 11 have been prepared by various synthetic methods, starting from the corresponding iodides or bromides. Methods based on sodium hydrogen sulfide, commonly used to accomplish this conversion, treatment of the Bunte salt obtained from sodium thiosulfate, the basic hydrolysis of isothiouronium salts, the hydrolysis under mild conditions of thiophosphorates formed from sodium thiophosphate and the basic hydrolysis of thiol acetic acid derivatives, have been investigated and compared relatively to the selective synthesis of the title compounds. The thiolacetic route yields essentially the thiols with some amounts of disulfides. Results from thiourea appears similar. Sodium thiophosphate constitutes an excellent route for the synthesis of thioethers, particularly when starting from the bromides. The two classical methods based on sodium hydrogen sulfide and sodium thiosulfate exhibit poor selectivity. It has been possible to obtain all the sulfur compounds reported in the pure state.