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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25298Generated: October 31, 2026

2-Fluoro-4-(4-trifluoromethylphenyl)benzonitrile → 2-Methylthio-4-(4-trifluoromethylphenyl)benzonitrile

https://huagongshe.com/reaction/25298

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-4-(4-trifluoromethylphenyl)benzonitrileHCID 22170924—
ReactantMethylmercaptan sodiumHCID 45051789—
SolventDimethylformamideHCID 6228—
Product2-Methylthio-4-(4-trifluoromethylphenyl)benzonitrileHCID 2217092275.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

To 3.0 g (11.3 mmol) of 2-fluoro-4-(4-trifluoromethylphenyl)benzonitrile in 50 ml of N,N-dimethylformamide, 7.0 g (15.0 mmol) of 15% aqueous sodium methyl mercaptan was added dropwise at room temperature. After 6 hours of stirring at 60° C., the reaction mixture was poured into 200 ml of ice-cold water and extracted with 100 ml of ethyl acetate twice. The ethyl acetate layer was washed with 100 ml of water twice and dried over anhydrous magnesium sulfate, and the ethyl acetate was distilled off under reduced pressure. Purification of the residue by silica gel column chromatography afforded 2.5 g of 2-methylthio-4-(4-trifluoromethylphenyl)benzonitrile (yield 75%) as white crystals (m.p. 128-129° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858639B2
Source datasetuspto-grants-2005_02
ORD IDord-ecd7c8d5ee06417d92c41a340d95960b
Source noteuspto-grants-2005_02