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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356826Generated: November 2, 2026

Carbon Dioxide → 3-Bromo-5-fluorobenzoic acid

https://huagongshe.com/reaction/1356826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
Reactant1,3-Dibromo-5-fluorobenzeneHCID 137003—
ReactantMagnesiumHCID 5462224—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product3-Bromo-5-fluorobenzoic acidHCID 277333955.4%

Reaction Steps

Magnesium turnings (1.97 g) and iodine (catalytic amount) were added to ether (150 ml), and 1,3-dibromo-5-fluorobenzene (19.6 g) in ether (20 ml) was added dropwise under nitrogen atmosphere at such a rate that gentle reflux occurred. The mixture was refluxed for 3 hours, and left to cool. Crushed dry ice was added thereto, and the mixture was stirred for 1 hour. The reaction mixture was poured into water, and acidified with hydrochloric acid. The mixture was extracted with ether (200 ml), and dried over magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (chloroform→chloroform:methanol=100:1), to thereby yield 9.37 g of the target compound (yield: 55.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586633B1
Source datasetuspto-grants-2003_07
ORD IDord-6775ff910faa4f119f70b65e6030ead4
Source noteuspto-grants-2003_07