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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494644Generated: October 25, 2026

Methanol → N-(4-chlorobutyl)-4-fluoro-N-(4-fluorophenyl)benzenamine

https://huagongshe.com/reaction/1494644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDimethyl SulfideHCID 1068—
ReactantBoraneHCID 6331—
Reactant4-chloro-N,N-bis(4-fluorophenyl)butanamideHCID 15087788—
SolventTetrahydrofuranHCID 8028—
ProductN-(4-chlorobutyl)-4-fluoro-N-(4-fluorophenyl)benzenamineHCID 1472255191.5%

Reaction Steps

To a stirred and cooled (0° C.) solution of 48 parts of 4-chloro-N,N-bis(4-fluorophenyl)butanamide in 108 parts of tetrahydrofuran were added 240 parts of a solution of borane, compound with thiobismethane, in tetrahydrofuran. After stirring overnight at room temperature, the reaction mixture was decomposed with 160 parts of methanol. After evaporation, The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and petroleum ether (20:80 by volume) as eluent. The pure fractions were collected and the eluent was evaporated, yielding 32.5 parts (91.5%) of N-(4-chlorobutyl)-4-fluoro-N-(4-fluorophenyl)benzeneamine as a residue (int. 70).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05026853
Source datasetuspto-grants-1991_06
ORD IDord-d2e5fc034c1d4792961653f083215c7d
Source noteuspto-grants-1991_06