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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 498941Generated: October 27, 2026

Water → 2-Cyclobutylmethylthio-4-(3-trifluoromethylpyrazolyl)benzonitrile

https://huagongshe.com/reaction/498941

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant(Bromomethyl)cyclobutaneHCID 2734658—
ReactantHCID 178509603HCID 178509603—
SolventDimethylformamideHCID 6228—
Product2-Cyclobutylmethylthio-4-(3-trifluoromethylpyrazolyl)benzonitrileHCID 17850960521.6%

Reaction Steps

0.9 g (3.3 mmol) of 2-mercapto-4-(3-trifluoromethylpyrazolyl)benzonitrile, 0.5 g (3.3 mmol) of cyclobutylmethyl bromide and 0.55 g (4.0 mmol) of potassium carbonate were stirred in 5 ml of N,N-dimethylformamide at room temperature overnight. The resulting reaction mixture was poured into 50 ml of water and the organic matters were extracted with 20 ml of ethyl acetate twice. The ethyl acetate layers were combined, then washed with 30 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 0.24 g of 2-cyclobutylmethylthio-4-(3-trifluoromethylpyrazolyl)benzonitrile (yield 21.2%) as a pale yellow powder (m.p. 102-103° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767626B2
Source datasetuspto-grants-2010_08
ORD IDord-84eda8357f904bd2a49041cb6a55a14d
Source noteuspto-grants-2010_08