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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066854Generated: October 26, 2026

Carbon tetrabromide → cis 4-(2-Fluoro-5-bromobenzyloxy)but-2-enyl bromide

https://huagongshe.com/reaction/1066854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
Reactant4-(2-Fluoro-5-bromobenzyloxy)but-2-en-1-olHCID 54380840—
SolventDiethyl EtherHCID 3283—
Productcis 4-(2-Fluoro-5-bromobenzyloxy)but-2-enyl bromideHCID 59958660—

Reaction Steps

In a 100 ml round bottom flask 4-(2-fluoro-5-bromobenzyloxy)but-2-en-1-ol (2.145 g, 7.80 mmol) was dissolved in diethyl ether under a nitrogen atmosphere. Triphenylphosphine (2.66 g, 10.1 mmol) and then carbon tetrabromide (3.36 g, 10.1 mmol) were added to the reaction mixture. The resulting mixture was stirred for six hours at ambient temperature. A white precipitate formed during the stirring. The progress of the reaction was monitored by thin layer chromatography. The solution was filtered and the filtrate was evaporated to give a thick oil. The desired title intermediate was further purified by liquid chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06245761B1
Source datasetuspto-grants-2001_06
ORD IDord-e41262f4ca1147f9a33952c021ccada0
Source noteuspto-grants-2001_06