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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 498950Generated: October 30, 2026

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

https://huagongshe.com/reaction/498950

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 numberUS07767626B2
Source datasetuspto-grants-2010_08
ORD IDord-368dedc3865c421d81d4a818cf4af432
Source noteuspto-grants-2010_08