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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1919482Generated: October 25, 2026

Carbon tetrabromide → 1-Bromo-4-(bromomethyl)-2,5-difluorobenzene

https://huagongshe.com/reaction/1919482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
Reactant(4-Bromo-2,5-difluorophenyl)methanolHCID 53401418—
SolventDichloromethaneHCID 6344—
Product1-Bromo-4-(bromomethyl)-2,5-difluorobenzeneHCID 2191121093.7%

Reaction Steps

To a solution of 2 g (8.44 mmol) of 4-bromo-2,5-difluorobenzoic acid (prepared according to the procedure of Ishikawa et al., Kogyo Kagaku Zasshi, pg 972-979, 1970) in 20 mL of tetrahydrofuran was added 40 mL of a 1M solution of borane-tetrahydrofuran complex. The solution was heated under reflux for 64 h, cooled to ambient temperature and 100 mL of methanol was added. The reaction was then heated for a further 2 h, cooled and concentrated in vacuo. Purification by flash chromatography (silica gel, 9:1 hexane:ethyl acetate) afforded 1.6 g of 4-bromo-2,5-difluorobenzyl alcohol. To a solution of 1.3 g (5.6 mmol) of 4-bromo-2,5-difluorobenzyl alcohol in 20 mL of dichloromethane at 0° C. was added 2.27 g (6.7 mmol) of carbon tetrabromide and 1.8 g (6.7 mmol) of triphenylphosphine. The reaction was stirred for 2 h at this temperature, the solvent was removed in vacuo and the residue stirred with 100 mL of diethyl ether. The solution was filtered, concentrated in vacuo, and purified by flash chromatography (silica gel, 9:1 hexane:ethyl acetate) to afford 1.5 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168637B2
Source datasetuspto-grants-2012_05
ORD IDord-41d424f9ea144483a9aac952414d7119
Source noteuspto-grants-2012_05