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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1955164Generated: November 1, 2026

Boron tribromide → 1,3-Benzenediol, 5-chloro-

https://huagongshe.com/reaction/1955164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
Reactant1-Chloro-3,5-dimethoxybenzeneHCID 81502—
SolventDichloromethaneHCID 6344—
Product1,3-Benzenediol, 5-chloro-HCID 9455458.6%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution 5-chloro-1,3-dimethoxybenzene (20.71 g) in dichloromethane (50 ml) at -78° C. was treated dropwise with a solution of boron tribromide (56 ml) in dichloromethane (250 ml), maintaining the temperature at -78° C. The mixture was slowly warmed to room temperature then left at ambient temperature for 48 hours. The reaction mixture was quenched with water (100 ml), (sodium hydroxide scrubber required) and partitioned between water (1000 ml) and dichloromethane (1000 ml). The organic layer was separated and the aqueous layer was extracted twice with a mixture of dichlioromethane and methanol (500 min, 98:2, v/v). The combined organic extracts were washed with saturated brine (200 ml), dried over magnesium sulphate and evaporated affording the title compound (10.17 g) as a yellow/orange oil which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06124343
Source datasetuspto-grants-2000_09
ORD IDord-15d9ffe7f97143f5a9807b2cbc96eaed
Source noteuspto-grants-2000_09