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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440535Generated: October 25, 2026

Water → 1-[4-(Trifluoromethoxy)phenyl]cyclobutanecarbonitrile

https://huagongshe.com/reaction/440535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,3-DibromopropaneHCID 8001—
ReactantSodium hydrideHCID 24758—
Reactant4-(Trifluoromethoxy)phenylacetonitrileHCID 142676—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product1-[4-(Trifluoromethoxy)phenyl]cyclobutanecarbonitrileHCID 2190207766.4%

Reaction Conditions

Temperature20 °C

Reaction Steps

A solution of 4-trifluoromethoxyphenylacetonitrile (38.9 g) and 1,3-dibromopropane (39.1 g) in tetrahydrofuran (50 ml) was added under argon to a stirred solution of 50% sodium hydride (19.2 g) in tetrahydrofuran (200 ml) and dimethylformamide (25 ml) at 25°-30° C. over 1 hour. The mixture was stirred at 20° C. for 1.5 hours, then at 30°-40° C. for 1 hour, then cooled and water added. The mixture was filtered and washed with ether. The organic layer was washed with water, dried over magnesium sulphate and the solvent removed by evaporation. The residue was distilled (b.p. 111°-117° C./10 mbar) to give 1-(4-trifluoromethoxyphenyl)cyclobutanecarbonitrile (30.98 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05519034
Source datasetuspto-grants-1996_05
ORD IDord-a510089955fd40b6a812525fcbad9149
Source noteuspto-grants-1996_05