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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784829Generated: October 29, 2026

Hydrogen Bromide → 3-Bromo-5-iodophenol

https://huagongshe.com/reaction/1784829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
Reactant1-Bromo-3-iodo-5-methoxybenzeneHCID 50998153—
CatalystTetrabutylammonium BromideHCID 74236—
SolventAcetic AcidHCID 176—
Product3-Bromo-5-iodophenolHCID 22630182352.9%

Reaction Steps

1-Bromo-3-iodo-5-methoxy-benzene (6.29 g, 20.1 mmol) was suspended in a solution of hydrogen bromide in acetic acid (33%, 150 mL). Tetrabutylammonium bromide (0.5 g, 1.55 mmol) was added and the mixture was heated to reflux under vigorous stirring for 2 d. After cooling to room temperature the mixture was extracted with methylene chloride (3×100 mL). The combined organic layers were washed with water (50 mL), dried (MgSO4) and concentrated to give the crude product which was purified by flash chromatography on silica gel (300 g, AcOEt/heptane 1:9). 3-Bromo-5-iodo-phenol (21.2 g, 96%) was obtained as pale brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504401B2
Source datasetuspto-grants-2009_03
ORD IDord-c82d30573024422aae1fd2c8d0f47fec
Source noteuspto-grants-2009_03