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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066838Generated: November 1, 2026

Carbon tetrabromide → 4-Bromo-2-(bromomethyl)-1-fluorobenzene

https://huagongshe.com/reaction/1066838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
Reactant(5-Bromo-2-fluorophenyl)methanolHCID 2773352—
SolventDiethyl EtherHCID 3283—
Product4-Bromo-2-(bromomethyl)-1-fluorobenzeneHCID 1355329576%

Reaction Steps

In a 250 ml round bottom flask, under a nitrogen atmosphere, 2-fluoro-5-bromobenzyl alcohol (5.85 g, 28.5 mmol) was dissolved in diethy ether (125 ml). To this solution triphenylphosphine (9.73 g, 37.1 mmol) and carbon tetrabromide (12.30 g, 37.1 mmol) were added. The resulting mixture was stirred at ambient temperature for about three hours. The progress of the reaction was monitored by thin layer chromatography. The mixture was then stirred at ambient temperature for about 19 additional hours. The reaction mixture was filtered and washed with cold diethyl ether. The filtrate was evaporated, yielding a light yellow oil. The oil was further purified by chromatography on a silica gel with hexanes. The desired fractions were purified by evaporation to yield 5.8 grams of the desired title intermediate. The material slowly crystallized upon standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06245761B1
Source datasetuspto-grants-2001_06
ORD IDord-6106027def1f48f59d1de82d9f8cf9a6
Source noteuspto-grants-2001_06