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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 886969Generated: October 30, 2026

Carbon Dioxide → 3-Bromo-2,6-difluorobenzoic acid

https://huagongshe.com/reaction/886969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantHydrochloric AcidHCID 313—
ReactantHexaneHCID 8058—
Reactant2,2,6,6-TetramethylpiperidineHCID 13035—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Bromo-2,4-difluorobenzeneHCID 67674—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product3-Bromo-2,6-difluorobenzoic acidHCID 14491596—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a mixed solution of 1.6N solution of n-butyllithium in hexane (9.4 ml, 15.0 mmol) and tetrahydrofuran (20 ml) were successively added 2,2,6,6-tetramethylpiperidine (2.50 ml, 15.0 mmol) and 1-bromo-2,4-difluorobenzene (2.90 g, 15.0 mmol) at −78° C., and the mixture was stirred at −78° C. for 1 hr. The pulverized dry ice (5 g) was added, and the mixture was stirred at −78° C. for 2 hr. Saturated aqueous ammonium chloride solution (5 ml) was added to the reaction mixture, and the mixture was stirred at room temperature for 30 min. Water (10 ml) and 1N hydrochloric acid (30 ml) were added, and the mixture was extracted with ethyl acetate. The extract was washed with water and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. Hexane was added to the residue, and desired product (2.30 g, 64.6%) was collected by filtration as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247403B2
Source datasetuspto-grants-2012_08
ORD IDord-719d73be3cbd4829b114b3a4133cd407
Source noteuspto-grants-2012_08