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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2045735Generated: November 2, 2026

Boron tribromide → 7-hydroxy-3-(4-hydroxyphenyl)-2H-chromen-2-one

https://huagongshe.com/reaction/2045735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
Reactant7-Hydroxy-3-(4'-methoxyphenyl)coumarinHCID 5393174—
SolventDichloromethaneHCID 6344—
Product7-hydroxy-3-(4-hydroxyphenyl)-2H-chromen-2-oneHCID 10244018—

Reaction Steps

4.00 g (14.9 mmol) of 7-hydroxy-3-(4-methoxyphenyl)chromen-2-one are initially introduced in 190 ml of dichloromethane, and a solution of 2.5 ml (26.3 mmol) of boron tribromide in 10 ml of dichloromethane is added with ice-cooling. The cooling is removed, and the batch is stirred overnight at room temp. The solution is added to ice-water, acidified using 2 N hydrochloric acid and extracted three times with ethyl acetate. The combined org. phases are washed with water and dried over sodium sulfate. The solvent is removed in vacuo, and the residue is recrystallised from toluene/ethyl acetate (2:1), giving 7-hydroxy-3-(4-hydroxyphenyl)chromen-2-one as yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592007B2
Source datasetuspto-grants-2013_11
ORD IDord-44f91c4a567545cf900c075a8adf01d9
Source noteuspto-grants-2013_11