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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109137Generated: October 30, 2026

Water → 4-Bromo-2,3-Dichlorophenol

https://huagongshe.com/reaction/2109137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDichloromethaneHCID 6344—
Reactant2,3-DichlorophenolHCID 11334—
ReactantBromineHCID 24408—
SolventAcetic AcidHCID 176—
SolventChloroformHCID 6212—
Product4-Bromo-2,3-DichlorophenolHCID 12311538—

Reaction Conditions

Temperature10 °C

Reaction Steps

In a 250 mL round bottom flask 10 g of 2,3-dichlorophenol was dissolved in a solvent mixture of glacial acetic acid (16 mL) and chloroform (4 mL) and cooled to 10° C. To this was added bromine (3.45 mL) in 15 mL of glacial acetic acid dropwise while maintaining the temperature. The reaction was vigorously stirred while adding bromine and continued stirring vigorously 0.5 h after addition was finished. At this time reaction mixture was poured into a flask containing 60 mL of water and 30 mL of dichloromethane. Organic layer was separated and aqueous layer was extracted with dichloromethane (3×50 mL). The oraganic layers were combined and washed with Sat. sodium bicarbonate (3×100 mL) and brine (100 mL) and dried over sodium sulfate. The crude product (9.65 g) was carried in to the next step without any purification. 1H-NMR (400 MHz, CDCl3) : 7.47 and 6.89 (ABq, 2H), 5.69 (brs, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514473B2
Source datasetuspto-grants-2009_04
ORD IDord-d7aa5c84af0a4be685d9c9601d48dbb6
Source noteuspto-grants-2009_04