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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093828Generated: November 1, 2026

Water → 2-Bromo-5-fluoro-4-methoxyphenol

https://huagongshe.com/reaction/2093828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBromineHCID 24408—
ReactantSodium SulfiteHCID 24437—
Reactant3-Fluoro-4-methoxyphenolHCID 14661613—
SolventDichloromethaneHCID 6344—
Product2-Bromo-5-fluoro-4-methoxyphenolHCID 66866569—

Reaction Conditions

Temperature-15 °C

Reaction Steps

3-Fluoro-4-methoxy-phenol (21.32 g; 0.15 mol) prepared according to literature [Freedman, J.; Stewart, K. T.; J. Heterocycl. Chem. 1989, 26, 1547-1554] is dissolved in dry dichloromethane (300 mL). The well stirred reaction mixture is cooled to −15° C. (ice/salt). A solution of bromine (23.97 g; 0.15 mol) in dry dichloromethane (75 mL) is slowly dropped into the reaction mixture. After complete addition stirring is continued for one hour. Water (150 mL) containing sodium sulfite (3.0 g) is added to the reaction mixture. Stirring is continued at ambient temperature for 30 min. The organic layer is separated, washed with water (100 mL) and dried over MgSO4 in the presence of decolorizing charcoal. After filtration the solvent is completely removed under reduced pressure. The residue is crystallized from tert-butylmethylether/hexane to give the title compound as a colorless solid. Yield: 30.74 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445501B2
Source datasetuspto-grants-2013_05
ORD IDord-d7af8c0bcc994df785a48a0f1c9ad94e
Source noteuspto-grants-2013_05