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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266558Generated: October 29, 2026

Carbon Dioxide → 4-Chloro-2-(trifluoromethyl)benzoic acid

https://huagongshe.com/reaction/266558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantHydrochloric AcidHCID 313—
Reactant4-Chloro-1-iodo-2-(trifluoromethyl)benzeneHCID 2724524—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
Product4-Chloro-2-(trifluoromethyl)benzoic acidHCID 2773856—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 4-chloro-2-trifluoromethyliodobenzene (100 g) in ether was added to a suspension of magnesium (8 g) in ether at a such a rate as to maintain the mixture at reflux. The mixture was stirred at reflux for 1 hour and then cooled to 0° C. Carbon dioxide was then passed into the stirred mixture for 3 hours. Hydrochloric acid (2M) was added and the resulting layers separated. The organic layer was washed with water and then extracted into aqueous sodium carbonate solution and this aqueous extract was acidified to pH 1 and extracted with ether. The ether layer was washed with saturated sodium chloride solution, dried (anhydrous magnesium sulphate) and the solvent evaporated to give 4-chloro-2-trifluoromethylbenzoic acid (57.1 g) as a brown solid, m.p. 106.5°-108° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05650533
Source datasetuspto-grants-1997_07
ORD IDord-43e5e965975f48cbb98b599a387aef85
Source noteuspto-grants-1997_07