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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822328Generated: November 1, 2026

Boron tribromide → 2-Phenoxy-3-trifluoromethyl-phenol

https://huagongshe.com/reaction/1822328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
Reactant2-Phenoxy-3-trifluoromethyl-anisoleHCID 69076100—
SolventDichloromethaneHCID 6344—
Product2-Phenoxy-3-trifluoromethyl-phenolHCID 5417285246%

Reaction Conditions

Temperature0 °C

Reaction Steps

A −78° C. solution of the crude 2-phenoxy-3-trifluoromethyl-anisole (3.47 g, 12.9 mmol) in CH2Cl2 (35 mL) is treated with BBr3 (12.99 g, 51.8 mmol), and the mixture is warmed to 0° C. and stirred for 1.5 h under N2. The reaction is poured into ice water and then extracted with Et2O. The organic layer is dried (Na2SO4), and the solvent is removed in vacuo to afford crude material that is absorbed on silica gel and columned with 96/4 chloroform/methyl tert-butyl ether to afford 1.51 g (24%) of 2-phenoxy-3-trifluoromethyl-phenol. Rf=0.34 (96/4 chloroform/methyl tert-butyl ether). 1H NMR (400 MHz, CDCl3); MS (ES−+) m/z mass calculated for C13H9O2F3 254, found 253 (M+1, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608639B2
Source datasetuspto-grants-2009_10
ORD IDord-924a77610ca34f3e91deb041e08a6521
Source noteuspto-grants-2009_10