HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 343000Generated: October 29, 2026
Carbon Dioxide → 4-Chloro-2-(trifluoromethyl)benzoic acid
https://huagongshe.com/reaction/343000
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Chloro-1-iodo-2-(trifluoromethyl)benzene | HCID 2724524 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-Chloro-2-(trifluoromethyl)benzoic acid | HCID 2773856 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05859283 |
|---|
| Source dataset | uspto-grants-1999_01 |
|---|
| ORD ID | ord-0718be8cb0b84232a6871ffb8e797c61 |
|---|
| Source note | uspto-grants-1999_01 |
|---|