Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414289Generated: October 25, 2026

Bromine → 4-Bromo-2,6-difluorophenol

https://huagongshe.com/reaction/414289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant2,6-DifluorophenolHCID 94392—
ReactantSodium PyrosulfiteHCID 656671—
CatalystHydrogen BromideHCID 260—
SolventCarbon DisulfideHCID 6348—
Product4-Bromo-2,6-difluorophenolHCID 273629223%

Reaction Steps

A solution of bromine (1.6 g) in dry carbon disulphide (10 cm3) was added over 5 minutes to a solution of 2,6-difluorophenol (1.3 g) in dry carbon disulphide (10 cm3). To the stirred reaction mixture was added 5 drops of 48% hydrogen bromide solution. The mixture was heated for 2 hours at the reflux temperature, then allowed to stand at the ambient temperature (ca 22° C.) for 16 hours. After a further period of heating (4 hours) the mixture was allowed to stand for 24 hours before being poured onto water (20 cm3). To the mixture was added saturated sodium metabisulphite solution (30 cm3). The layers were separated, and the organic phase was washed with saturated sodium hydrogen carbonate solution (20 cm3) and water (20 cm3). The organic layer was dried over anhydrous sodium sulphate then evaporated under reduced pressure to given an oil which solidified. The crude product was distilled in a Kugelrohr apparatus at an oven temperature of 100° C. under reduced pressure (ca. 20 mmHg). The distillate crystallised to give 4-bromo-2,6-difluorophenol as a white solid (0.48 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04791139
Source datasetuspto-grants-1988_12
ORD IDord-8d57ff4a88dd470dbf173fb2bf1d48af
Source noteuspto-grants-1988_12