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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069645Generated: October 30, 2026

Bromine → 5-Bromo-2,3-dihydro-2,2-dimethylbenzofuran-7-carboxylic acid

https://huagongshe.com/reaction/2069645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantSodium SulfiteHCID 24437—
Reactant2,2-Dimethyl-2,3-dihydro-1-benzofuran-7-carboxylic acidHCID 2795469—
SolventAcetic AcidHCID 176—
Product5-Bromo-2,3-dihydro-2,2-dimethylbenzofuran-7-carboxylic acidHCID 14838401—

Reaction Steps

Using a dropping funnel, bromine (0.8 mL, 15.6 mmol) in acetic acid (6 mL) was added to a solution of 2,2-dimethyl-2,3-dihydrobenzofuran-7-carboxylic acid (1 g, 5.20 mmol) in acetic acid at 0° C. The reaction was allowed to warm to room temperature and stirred overnight. A 2M solution of sodium sulfite was added until all of the red color disappeared. The volatiles were removed in vacuo and dichloromethane was added and the layers separated. The organic phase was washed with water and brine, dried over sodium sulfate, filtered and concentrated in vacuo to yield 5-bromo-2,2-dimethyl-2,3-dihydrobenzofuran-7-carboxylic acid (667).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299117B2
Source datasetuspto-grants-2012_10
ORD IDord-40dcec78394e4eb6aef70cef892ee377
Source noteuspto-grants-2012_10