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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25288Generated: October 30, 2026

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

https://huagongshe.com/reaction/25288

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 (B 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 numberUS06858639B2
Source datasetuspto-grants-2005_02
ORD IDord-2287a12e884b462b847ca54a0969e0df
Source noteuspto-grants-2005_02