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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583362Generated: November 1, 2026

Carbon Dioxide → 5-Bromo-3-methyl-1-benzothiophene-2-carboxylic acid

https://huagongshe.com/reaction/1583362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantDiisopropylamineHCID 7912—
Reactant5-Bromo-3-methyl-1-benzothiopheneHCID 14175764—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product5-Bromo-3-methyl-1-benzothiophene-2-carboxylic acidHCID 20260919—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A mixture of diisopropylamine (4.44 g.) and potassium t-butoxide (5.02 g.) in dry ether was cooled to -78° C. under an atmosphere of dry nitrogen and n-butyl lithium (28.4 ml. of 1.55M solution in hexane) was added with stirring over 5 minutes. The mixture was stirred at -78° for 30 minutes and then a solution of 5-bromo-3-methylbenzo[b]thiophene (9.10 g.) in dry ether (25 ml.) was added over 5 minutes. The resulting mixture was stirred at -78° C. for 30 minutes and then poured onto a mixture of crushed solid carbon dioxide and ether. When all the carbon dioxide had evaporated the mixture was shaken with water and the ether layer was separated. The aqueous layer was acidified with acetic acid and the solid was filtered off, washed with water and crystallized from acetic acid to give 5-bromo-3-methylbenzo[b]thiophene-2-carboxylic acid (7.30 g.), m.p. >300°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04551468
Source datasetuspto-grants-1985_11
ORD IDord-22307a9970fb420da9660e3af8ec741b
Source noteuspto-grants-1985_11