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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480655Generated: October 25, 2026

Boron tribromide → 3-Fluoro-4-methylphenol

https://huagongshe.com/reaction/480655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
Reactant3-Fluoro-4-methylanisoleHCID 2774571—
SolventDichloromethaneHCID 6344—
Product3-Fluoro-4-methylphenolHCID 277461375.2%

Reaction Conditions

Temperature-70 °C

Reaction Steps

To a −70° C. solution of 3-fluoro-4-methyl anisole (1.62 g; 11.6 mmol) in CH2Cl2 (10 mL) was added dropwise BBr3 (10 mL; 12 mmol). The reaction mixture was stirred at −70° C. for 10 min, then allowed to warm to 0° C. and stirred at 0° C. for 2 h. The reaction was allowed to warm to RT and concentrated in vacuo and the residue was partitioned between H2O and EtOAc. The organic phase was washed with H2O, dried (Na2SO4) and concentrated in vacuo to give 3-fluoro-4-methyl phenol (1.1 g; 75%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06653314B2
Source datasetuspto-grants-2003_11
ORD IDord-773cb28411f74f21b62a1ac81b99ead0
Source noteuspto-grants-2003_11