processo para a alquilação de derivados de alquil- ou benzilcianogênio na presença de trialquilaminas ou -fosfinas

Preparation of an alpha , alpha -disubstituted benzyl cyanide (I) involves reacting an alpha -unsubstituted or alpha -monosubstituted analog (II) with an alkylating agent in presence of a base and a tertiary amine or phosphine. Preparation of an alpha , alpha -disubstituted benzyl cyanide of formula...

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Main Authors RUDOLF LEHNERT, GERHARD KORB, HANS-WOLFRAM FLEMMING
Format Patent
LanguagePortuguese
Published 01.12.2009
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Abstract Preparation of an alpha , alpha -disubstituted benzyl cyanide (I) involves reacting an alpha -unsubstituted or alpha -monosubstituted analog (II) with an alkylating agent in presence of a base and a tertiary amine or phosphine. Preparation of an alpha , alpha -disubstituted benzyl cyanide of formula (I) involves reacting an alpha -unsubstituted or alpha -monosubstituted analog of formula (II) (optionally previously dissolved in an organic solvent) with an alkylating agent of formula R1-X (III) or X-CH2CH2-Z-(CH2)n-X (III') in presence of a base and a tertiary amine or phosphine of formula R7-Q(R8)(R9) (IV). R1 = 1-20C alkyl (optionally substituted by 1-3 Q' or phenyl (itself optionally substituted by 1-3 A or Q')) or 2-20C alkenyl (optionally substituted by 1-3 Q' or phenyl (itself optionally substituted by 1-3 A or Q')); R2 = as R1 or phenyl (optionally substituted by 1-3 Q' A); or R1 + R2 = -CH2CH2-Z-(CH2)n-; R3 = phenyl (optionally substituted by 1-3 A or Q'); R4 = H or as R2; A = 1-6C alkyl; Q' = 3-6C cycloalkyl, OH, ACOO, AO, (1-6C) alkoxy-(1-4C) alkoxy, halo, CF3, CN, NO2, COOH, AOCO, OCH2O, NR5R6CO or NR5R6; R5, R6 = H or A; Z = O, S or NR; R = H, A, benzyl or phenyl; n = 1 or 2; X = halo or 1/2 SO4; R7-R9 = 1-30C alkyl or phenyl; Q = N or P.
AbstractList Preparation of an alpha , alpha -disubstituted benzyl cyanide (I) involves reacting an alpha -unsubstituted or alpha -monosubstituted analog (II) with an alkylating agent in presence of a base and a tertiary amine or phosphine. Preparation of an alpha , alpha -disubstituted benzyl cyanide of formula (I) involves reacting an alpha -unsubstituted or alpha -monosubstituted analog of formula (II) (optionally previously dissolved in an organic solvent) with an alkylating agent of formula R1-X (III) or X-CH2CH2-Z-(CH2)n-X (III') in presence of a base and a tertiary amine or phosphine of formula R7-Q(R8)(R9) (IV). R1 = 1-20C alkyl (optionally substituted by 1-3 Q' or phenyl (itself optionally substituted by 1-3 A or Q')) or 2-20C alkenyl (optionally substituted by 1-3 Q' or phenyl (itself optionally substituted by 1-3 A or Q')); R2 = as R1 or phenyl (optionally substituted by 1-3 Q' A); or R1 + R2 = -CH2CH2-Z-(CH2)n-; R3 = phenyl (optionally substituted by 1-3 A or Q'); R4 = H or as R2; A = 1-6C alkyl; Q' = 3-6C cycloalkyl, OH, ACOO, AO, (1-6C) alkoxy-(1-4C) alkoxy, halo, CF3, CN, NO2, COOH, AOCO, OCH2O, NR5R6CO or NR5R6; R5, R6 = H or A; Z = O, S or NR; R = H, A, benzyl or phenyl; n = 1 or 2; X = halo or 1/2 SO4; R7-R9 = 1-30C alkyl or phenyl; Q = N or P.
Author RUDOLF LEHNERT
GERHARD KORB
HANS-WOLFRAM FLEMMING
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Snippet Preparation of an alpha , alpha -disubstituted benzyl cyanide (I) involves reacting an alpha -unsubstituted or alpha -monosubstituted analog (II) with an...
SourceID epo
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SubjectTerms ACYCLIC OR CARBOCYCLIC COMPOUNDS
AMMONIA
APPARATUS THEREFOR
CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOIDCHEMISTRY
CHEMISTRY
COMPOUNDS THEREOF
CYANOGEN
GENERAL METHODS OF ORGANIC CHEMISTRY
HETEROCYCLIC COMPOUNDS
INORGANIC CHEMISTRY
METALLURGY
ORGANIC CHEMISTRY
PERFORMING OPERATIONS
PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
THEIR RELEVANT APPARATUS
TRANSPORTING
Title processo para a alquilação de derivados de alquil- ou benzilcianogênio na presença de trialquilaminas ou -fosfinas
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