HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342976Generated: October 30, 2026
Carbon Dioxide → 2-Chloro-4-(trifluoromethoxy)benzoic acid
https://huagongshe.com/reaction/342976
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | 1-Bromo-2-chloro-4-(trifluoromethoxy)benzene | HCID 53414034 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Chloro-4-(trifluoromethoxy)benzoic acid | HCID 54190493 | — |
Reaction Steps
n-Butyllithium (2.5M in hexane, 38 ml) was added to a stirred, cooled solution of 2-chloro-4-trifluoromethoxybromobenzene (25 g) in ether while maintaining the temperature below -70° C. The mixture was stirred at -78° C. for 4 hours then poured onto solid carbon dioxide with stirring. The mixture was allowed to warm to room temperature and acidified to pH1. The layers were separated and the organic layer was washed with water, dried (MgSO4) and filtered. The filtrate was evaporated to dryness and the residue was triturated with cyclohexane and filtered to give 2-chloro-4-trifluoromethoxybenzoic acid as a white solid mp 90.6°-91.2° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05859283 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-7651f9372baa45618372694f28087396 |
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| Source note | uspto-grants-1999_01 |
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