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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1385645Generated: October 31, 2026

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

https://huagongshe.com/reaction/1385645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantBromineHCID 24408—
Reactant4-(4-Chlorophenyl)-2-fluoro-4-methylpent-2-enolHCID 53791045—
SolventCarbon TetrachlorideHCID 5943—
Product1-Bromo-4-(p-chlorophenyl)-2-fluoro-4-methyl-2-penteneHCID 5373947971%

Reaction Steps

Under a nitrogen atmosphere, a solution of triphenyl phosphine (0.96 g, 4.25 mmol) in carbon tetrachloride at −5° C. is treated dropwise with a solution of bromine (0.679 g, 4.25 mmol) in carbon tetrachloride, warmed to and stirred at room temperature for 45 minutes, treated with a solution of 4-(p-chlorophenyl)-2-fluoro-4-methyl-2-penten-1-ol, (Z)—(0.81 g, 3.54 mmol) in carbon tetrachloride, refluxed for 2 hours, cooled to room temperature, and poured into petroleum ether. The resultant mixture is filtered through diatomaceous earth. The filtrate is washed sequentially with water, saturated sodium hydrogen carbonate solution and brine, dried over anhydrous sodium sulfate and concentrated in vacuo to obtain an oil. Flash column chromatography of the oil using silica gel and a 1:9 ethyl acetate/hexanes solution gives the title product as a colorless oil (0.736 g, 71% 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-4d13f5869fb14839be54002baccf8943
Source noteuspto-grants-2001_07