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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458388Generated: November 2, 2026

Triphenylphosphine → 1-Bromo-4-(p-chlorophenyl)-3-fluoro-4-methyl-2-pentene

https://huagongshe.com/reaction/1458388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantBromineHCID 24408—
ReactantEthyl acetate hexaneHCID 21226206—
Reactant4-(p-Chlorophenyl)-3-fluoro-4-methyl-2-penten-1-olHCID 54566349—
SolventCarbon TetrachlorideHCID 5943—
Product1-Bromo-4-(p-chlorophenyl)-3-fluoro-4-methyl-2-penteneHCID 5427291392.6%

Reaction Steps

A solution of triphenyl phosphine (12.58 g, 55.6 mmol) in carbon tetrachloride at -5° C. to 5° C. is treated dropwise with a solution of bromine (8.89 g, 55.6 mmol) in carbon tetrachloride over 50 minutes under nitrogen, stirred at room temperature for one hour, treated with a solution of 4-(p-chlorophenyl)-3-fluoro-4-methyl-2-penten-1-ol, (Z)- (10.6 g, 46.3 mmol) in carbon tetrachloride over 15 minutes, refluxed for 2.5 hours, cooled to room temperature, and poured into petroleum ether. The resultant mixture is filtered through diatomaceous earth and concentrated in vacuo to obtain a residue. Flash chromatography of the residue using silica gel and a 1:9 ethyl acetate/hexane solution gives the title product as an oil (12.5 g, 92.6% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05849958
Source datasetuspto-grants-1998_12
ORD IDord-c6c811954e764a9d86e4acbf93299fa1
Source noteuspto-grants-1998_12