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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 431389Generated: October 30, 2026

Boron tribromide → 4-Bromo-3-nitrophenol

https://huagongshe.com/reaction/431389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
Reactant4-Bromo-3-nitroanisoleHCID 79288—
SolventDichloromethaneHCID 6344—
Product4-Bromo-3-nitrophenolHCID 1581786768.8%

Reaction Steps

To a stirred solution of 1-bromo-4-methoxy-2-nitrobenzene (2.32 g, 10 mmol) in 75 mL of dichloromethane at 0° C. was added BBr3 solution (1 M in DCM, 12 mL, 12 mmol) dropwise. The solution was allowed to warm to room temperature and stirred for 16 h. GC/MS showed starting material still left so another 12 mL of BBr3 solution was added and the reaction mixture refluxed for 4 h. The reaction mixture was cooled in ice and quenched with water. After washing successively with saturated NaHCO3(aq) and brine, the organic layer was dried over MgSO4, filtered and evaporated. The resulting yellow solid was flash chromatographed (25% EtOAc/hexane) to give 1.5 g of product in (69%) yield as a pale yellow solid: MS (EI) m/z 218 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06656971B2
Source datasetuspto-grants-2003_12
ORD IDord-104232f3e11146ffb929231e07ad212a
Source noteuspto-grants-2003_12