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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782592Generated: October 30, 2026

Bromide ion → 5-bromo-2-chloro-4-fluoroanisole

https://huagongshe.com/reaction/1782592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
ReactantDichloromethaneHCID 6344—
Reactant4-Chloro-2-fluoro-5-methoxyanilineHCID 185082—
ReactantSodium NitriteHCID 23668193—
SolventHydrogen BromideHCID 260—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product5-bromo-2-chloro-4-fluoroanisoleHCID 1022037849%

Reaction Steps

A solution of 4-chloro-2-fluoro-5-methoxyaniline (25.0 g, 0.143 mol) in 10% HBr (250 mL) was cooled to 0° C. and a solution of sodium nitrite (15.0 g, 0.218 mol) in water (20 mL) was slowly added. Methylene chloride (50 mL) and curpric bromide (30.0 g, 0.244 mol) were added slowly and then the mixture was warmed to ambient temperature and stirred for 1 hour. The reaction mixture was filtered through a bed of celite and extracted with methylene chloride (2×100 mL) and the combined organic phases were dried (sodium sulfate) and concentrated. Chromatography of the dark oil (5% ethyl acetate in hexanes) gave 1-bromo-4-chloro-2-fluoro-5-methoxybenzene (16.6 g, 0.070 mol): 1H NMR (CDCl3): δ 7.20 (m, 1H) 7.05 (dd, 1H), 4.00 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498468B2
Source datasetuspto-grants-2009_03
ORD IDord-9e31a094b5ad4c52a5d3d502c4b2d626
Source noteuspto-grants-2009_03