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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635726Generated: November 2, 2026

Sodium Hydroxide → 2-Cyclopropylmethylthio-4-(5-trifluoromethylpyridin-2-yl)benzonitrile

https://huagongshe.com/reaction/1635726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant[(Cyclopropylmethyl)sulfanyl]methanimidamide hydrobromideHCID 2777025—
ReactantHCID 22170891HCID 22170891—
SolventDimethylformamideHCID 6228—
Product2-Cyclopropylmethylthio-4-(5-trifluoromethylpyridin-2-yl)benzonitrileHCID 2217089496.8%

Reaction Steps

1.8 g (6.8 mmol) of 4-(5-trifluoromethylpyridin-2-yl)-2-fluorobenzonitrile, 1.6 g (7.6 mmol) of S-cyclopropylmethylisothiourea hydrobromide salt and 50 ml of N,N-dimethylformamide were put into a round-bottomed flask and stirred together with 1.6 g (8 mmol) of 20% aqueous sodium hydroxide overnight. The solvent was distilled off under reduced pressure, and the reaction mixture was separated with 50 ml of water and 50 ml of ethyl acetate. The organic layer was washed with 50 ml of water twice and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure to obtain 2.2 g of 2-cyclopropylmethylthio-4-(5-trifluoromethylpyridin-2-yl)benzonitrile (yield 96%) as pale yellow feathery crystals (m.p. 135-136° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06509354B1
Source datasetuspto-grants-2003_01
ORD IDord-1f91e9377c9b479cac3361b97148362a
Source noteuspto-grants-2003_01