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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1385643Generated: October 29, 2026

Triphenylphosphine → 1-(p-Chlorophenyl)-1-(3-bromo-2-fluoropropenyl)cyclopropane

https://huagongshe.com/reaction/1385643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantBromineHCID 24408—
Reactant1-(4-Chlorophenyl)-1-(2-fluoro-3-hydroxyprop-1-enyl) cyclopropaneHCID 54354973—
SolventCarbon TetrachlorideHCID 5943—
Product1-(p-Chlorophenyl)-1-(3-bromo-2-fluoropropenyl)cyclopropaneHCID 5376576463%

Reaction Steps

Under a nitrogen atmosphere, a solution of bromine (0.767 g, 4.8 mmol) in carbon tetrachloride at ice-water bath temperature is treated sequentially with a solution of triphenylphosphine (1.26 g, 4.8 mmol) in carbon tetrachloride and a solution of 3-[1-(p-chlorophenyl)-cyclopropyl]-2-fluoro-2-propen-1-ol, (Z)—(0.907 g, 4 mmol) in carbon tetrachloride, heated to and stirred at reflux for 70 minutes, cooled to room temperature, and poured into petroleum ether. The resultant mixture is filtered, and the filtrate is concentrated in vacuo to obtain a residue. The residue is dissolved in petroleum ether and passed through a plug of silica gel (eluted with hexanes) to obtain an oil. Flash column chromatography of the oil using silica gel and a 3:20 methylene chloride/hexanes solution gives the title product as a colorless oil (0.73 g, 63% yield) which is identified by NMR spectral analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06262319B1
Source datasetuspto-grants-2001_07
ORD IDord-b051a02e5b6d4031a2147734b6c2ffb3
Source noteuspto-grants-2001_07