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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1920804Generated: October 29, 2026

Methanol → 1-(2-Bromo-3-hydroxyphenyl)ethanone

https://huagongshe.com/reaction/1920804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPhosphorus tribromideHCID 24614—
ReactantHCID 19702329HCID 19702329—
SolventDichloromethaneHCID 6344—
Product1-(2-Bromo-3-hydroxyphenyl)ethanoneHCID 2321696247%

Reaction Conditions

Temperature-40 °C

Reaction Steps

Under a nitrogen atmosphere, 1-(2-bromo-3-methoxy phenyl)ethanone (30.5 g, 229 mmol) which had been obtained in Reference example 3 (3b) was dissolved in methylene chloride (500 mL), and added dropwise with a 1.0 M solution of tribromo phosphine in dichloromethane (293 mL, 293 mmol) at −80° C. over 5 hours. Upon the completion of the dropwise addition, the mixture was stirred for 17 hours at −40° C. Subsequently, the reaction solution was cooled to −80° C. and added dropwise with methanol (500 mL). Upon the completion of the dropwise addition, the temperature was raised to −40° C. followed by stirring for 3 hours. The temperature of the reaction solution was raised to room temperature. The solvent was distilled off under reduced pressure until the solution turned green. After adding ethanol, the mixture was extracted with ethyl acetate/hexane (1:1, V/V). After neutralization with a saturated aqueous solution of sodium hydrogen carbonate, the solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography (hexane:ethyl acetate, 100:0-55:45, V/V) to give the title compound as a colorless oily substance (13.5 g, yield 47%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173631B2
Source datasetuspto-grants-2012_05
ORD IDord-7617058e45494fd2a7bb1858fe0424a3
Source noteuspto-grants-2012_05