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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351559Generated: November 2, 2026

Bromoform → 1,1-Dibromo-2-(3,4-dichlorophenyl)cyclopropane

https://huagongshe.com/reaction/2351559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoformHCID 5558—
Reactant3,4-DichlorostyreneHCID 74869—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
Product1,1-Dibromo-2-(3,4-dichlorophenyl)cyclopropaneHCID 19818501—

Reaction Conditions

Temperature-30 °C

Reaction Steps

Potassium t-butoxide (5.1 g.) was added to a stirred mixture of 3,4-dichlorophenylethylene (6.1 g.), bromoform (8.9 g.) and petroleum ether (b.p. 60°-80° C.; 100 ml.) which was cooled to -30° C., and the mixture was stirred at that temperature for 30 minutes, then at laboratory temperature for 17 hours and then poured into water. The mixture was extracted with ethyl acetate and the extract was washed with saturated aqueous sodium chloride solution, dried over magnesium sulphate and evaporated to dryness under reduced pressure. The residue was purified by chromatography on a silica gel column using petroleum ether (b.p. 40°-60° C.) as eluant, and there was thus obtained as an oil 1,1-dibromo-2-(3,4-dichlorophenyl)cyclopropane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04873329
Source datasetuspto-grants-1989_10
ORD IDord-54f787ba4f5a4186a7ea3e390e9be1cc
Source noteuspto-grants-1989_10