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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896178Generated: October 30, 2026

Water → 2-(4-Bromophenyl)oxirane

https://huagongshe.com/reaction/1896178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
Reactant4-BromobenzaldehydeHCID 70741—
ReactantTrimethylsulfonium iodideHCID 75127—
SolventAcetonitrileHCID 6342—
Product2-(4-Bromophenyl)oxiraneHCID 119460—

Reaction Conditions

Temperature55 °C

Reaction Steps

A mixture of 4-bromobenzaldehyde (intermediate 29, 25.25 g, 136 mmol), trimethylsulfonium iodide (28.71 g, 141 mmol), water (6.5 ml, 361 mmol) and potassium hydroxide (15.56 g, 277 mmol) in acetonitrile (140 ml) was warmed to 55° C. for 2.5 hours. The resulting solution was partitioned between water and diethyl ether, and the organic layer was washed with water, diluted hydrochloric acid, and brine, and dried over sodium sulfate. Crude product of 2-(4-bromo-phenyl)-oxirane (intermediate 30) was obtained by removal of organic solvent under reduced pressure, which was used for next reaction without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518939B2
Source datasetuspto-grants-2013_08
ORD IDord-d7cab41c7f8f456abd7dda259516473b
Source noteuspto-grants-2013_08