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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266864Generated: November 1, 2026

Bromine → 2-Bromo-1-[1-(3,4-dichlorophenyl)cyclobutyl]ethan-1-one

https://huagongshe.com/reaction/266864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant1-Acetyl-1-(3,4-dichlorophenyl)cyclobutaneHCID 13083139—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
Product2-Bromo-1-[1-(3,4-dichlorophenyl)cyclobutyl]ethan-1-oneHCID 21258472—

Reaction Steps

A solution of bromine (18 ml) in chloroform (80 ml) was added dropwise at 10°-15° C. over 1.5 hours to a stirred solution of the above 1-[1-(3,4-dichlorophenyl)-cyclobutyl]ethanone (89.6 g) in a mixture of methanol (120 ml) and chloroform (20 ml). When the addition was complete, the mixture was stirred at ambient temperature for 1 hour, then poured onto an excess of ice-water. The aqueous layer was separated and the product extracted into dichloromethane (2×150 ml). The combined organic solutions were washed with saturated aqueous sodium hydrogen carbonate solution (2×200 ml) then with water, dried over calcium chloride and the solvent removed in vacuo to yield an oil. The oil was distilled to give 2-bromo-l-[1-(3,4-dichlorophenyl)-cyclobutyl]ethanone (88.31 g), b.p. 148°-154° C./0.66 mbar.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05652271
Source datasetuspto-grants-1997_07
ORD IDord-8a7d85cdad364527ad469952f7984b55
Source noteuspto-grants-1997_07