Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700911Generated: October 31, 2026

Boron tribromide → 1,1,1-Trifluoro-4-(4-hydroxyphenyl)butan-2-one

https://huagongshe.com/reaction/1700911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
Reactant1,1,1-Trifluoro-4-(4-methoxy-phenyl)-butan-2-oneHCID 15449107—
ReactantAcetone cardiceHCID 18522661—
SolventDichloromethaneHCID 6344—
Product1,1,1-Trifluoro-4-(4-hydroxyphenyl)butan-2-oneHCID 19524484.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1,1,1-trifluoro-4-[4-methoxyphenyl]-2-butanone (43.5 g, 0.187 mol) in dichloromethane (500 ml) at −78° C. (dry ice-acetone) was added dropwise boron tribromide (53 ml, 0.561 mol). The mixture was then stirred at 0° C. (ice bath) for 3 h, and cautiously quenched by dropwise addition of ice-water (200 ml) over a period of 1 h. The aqueous phase was saturated with solid sodium chloride, extracted with dichloromethane (500 ml) followed by diethyl ether (500 ml). The combined organic layers were dried over anhydrous magnesium sulfate and concentrated in vacuo. The residue was purified by bulb-to-bulb distilation (96-100° C., 0.2 mmHg) to afford the title compound (34.4 g, 84%) as a yellow liquid which solidified upon standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350892B1
Source datasetuspto-grants-2002_02
ORD IDord-8041ce92f2614c57baa53366cf6ef00e
Source noteuspto-grants-2002_02