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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 498960Generated: October 30, 2026

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

https://huagongshe.com/reaction/498960

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 numberUS07767626B2
Source datasetuspto-grants-2010_08
ORD IDord-4d56f78854aa46868128c4d24efb12ee
Source noteuspto-grants-2010_08