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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946401Generated: November 1, 2026

Phosphorus tribromide → 2-(Bromomethyl)-4-(phenyloxy)-1-(trifluoromethyl)benzene

https://huagongshe.com/reaction/1946401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus tribromideHCID 24614—
ReactantSodium BicarbonateHCID 516892—
Reactant[5-(Phenyloxy)-2-(trifluoromethyl)phenyl]methanolHCID 66770967—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2-(Bromomethyl)-4-(phenyloxy)-1-(trifluoromethyl)benzeneHCID 6677072469.8%

Reaction Conditions

Temperature-5 °C

Reaction Steps

[5-(phenyloxy)-2-(trifluoromethyl)phenyl]methanol (0.493 g, 1.84 mmol) in dichloromethane (12 ml) under nitrogen was stirred and cooled to −5° C. A solution of phosphorus tribromide (173 μl, 1.84 mmol) in DCM (3.5 ml) was added dropwise over about 2 min. The solution was then allowed to warm to room temperature and left to stand overnight. The solution was cooled to 4° C. and stirred well as saturated aqueous sodium bicarbonate (11 ml) was added in portions over 2 min. The biphasic mixture was stirred for a further 20 min. The mixture was diluted with water and DCM. The phases were separated using a hydrophobic frit and the aqueous phase washed with DCM. The combined organic extracts were stored in a freezer over the weekend and the DCM solution decanted off from crystals of ice. The organic phase was further dried (MgSO4), filtered and the solvent removed in vacuo to leave crude 2-(bromomethyl)-4-(phenyloxy)-1-(trifluoromethyl)benzene as a colourless oil (0.425 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399436B2
Source datasetuspto-grants-2013_03
ORD IDord-ed38c72a2f274fe59143cc8971372b1d
Source noteuspto-grants-2013_03