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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173291Generated: October 30, 2026

Lithium hydroxide, monohydrate → 7-bromobenzofuran-3-carboxylic acid

https://huagongshe.com/reaction/2173291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantHCID 21694197HCID 21694197—
SolventMethanol tetrahydrofuran waterHCID 21892291—
Product7-bromobenzofuran-3-carboxylic acidHCID 65669528—

Reaction Steps

To a solution of ethyl 7-bromo-1-benzofuran-3-carboxylate (1.0 g, 3.7 mmol) in 20 mL of MeOH/THF/H2O (2/211) was added LiOH H2O (777 mg, 18.5 mmol), and the mixture was stirred at ambient temperature overnight. The solvents were removed under vacuum, and the residue was added 10 mL of water and extracted with ether (100 mL). The aqueous layer was then acidified with 4 N HCl to pH=3 in ice bath, and extracted with EtOAc. The combined organic phase was washed with brine, dried over anhydrous sodium sulfate and concentrated to give 7-bromo-1-benzofuran-3-carboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056859B2
Source datasetuspto-grants-2015_06
ORD IDord-c5eef8cc7c504d9ba82c9937127bdd2e
Source noteuspto-grants-2015_06