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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523233Generated: October 26, 2026

Carbon Dioxide → 4-Bromo-2,5-difluorobenzoic acid

https://huagongshe.com/reaction/523233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
Reactant1,4-Dibromo-2,5-difluorobenzeneHCID 67596—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product4-Bromo-2,5-difluorobenzoic acidHCID 82285753%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 1,4-dibromo-2,5-difluorobenzene (640 mg, 2.35 mmol) in dry diethyl ether (10 mL) cooled in a dry ice-acetone bath was treated dropwise with 2.5 M n-butyllithium in hexanes (1.04 mL, 2.59 mmol). The solution was stirred at −78° C. for 30 min, then was treated with a piece of dry ice. The cooling bath was removed after 5 min and the mixture was stirred for another 30 min while warming to room temperature. The mixture was diluted with EtOAc and water. The organic phase was separated and washed twice with saturated aqueous NaHCO3. The combined aqueous phases were acidified with 1M aqueous HCl, extracted twice with DCM, and the combined organic phases were dried and concentrated to give 4-bromo-2,5-difluorobenzoic acid as a white solid (297 mg, 53% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334290B2
Source datasetuspto-grants-2016_05
ORD IDord-5e76969404fd4db6871fcd7917306608
Source noteuspto-grants-2016_05