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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175878Generated: November 1, 2026

Carbon Dioxide → 4-Bromo-2-fluoro-3-methoxybenzoic acid

https://huagongshe.com/reaction/2175878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantDiisopropylamineHCID 7912—
Reactant1-Bromo-3-fluoro-2-methoxybenzeneHCID 16102688—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product4-Bromo-2-fluoro-3-methoxybenzoic acidHCID 16102676—

Reaction Conditions

Temperature0 °C

Reaction Steps

n-BuLi (17.0 mL, 42.5 mmol) was added dropwise to the solution of NH(i-Pr)2 (4.50 g, 44.5 mmol) in 70 mL of THF at −70° C. The mixture was stirred at 0° C. for 15 minutes and then cooled to −70° C. again. The solution of 1-bromo-3-fluoro-2-methoxybenzene (8.30 g, 40.5 mmol, in 30 mL of THF) was added dropwise. The resulting mixture was stirred at −70° C. for 1 hour then poured into fresh dry ice and stirred overnight. The mixture was diluted with 1 L of ether and washed with water twice. The combined water layer was washed with ether then acidified to pH=2 with hydrochloric acid and extracted with EtOAc twice. The combined EtOAc layer was washed with brine, dried over anhydrous Na2SO4 and concentrated to give 4-bromo-2-fluoro-3-methoxybenzoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062070B2
Source datasetuspto-grants-2015_06
ORD IDord-de2c830ba13f49369f848f08ff037fd2
Source noteuspto-grants-2015_06