HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613966Generated: November 3, 2026
1-Chloro-4-(trifluoromethyl)benzene → 4-(Trifluoromethyl)benzoic acid
https://huagongshe.com/reaction/1613966
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Chloro-4-(trifluoromethyl)benzene | HCID 7394 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Catalyst | 1,4-Bis(diphenylphosphino)butane | HCID 82124 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(Trifluoromethyl)benzoic acid | HCID 9966 | 265.6% |
Reaction Steps
In an autoclave made of glass were placed 180.6 g of parachlorobenzotrifluoride, 0.64 g of 5% palladium-carbon, 4.3 g of 1,4-bisdiphenylphosphinobutane and 21.2 g of sodium carbonate. The air in the autoclave was replaced with carbon monoxide introduced thereinto several times, after which carbon monoxide was further introduced to adjust its pressure therein to 10 kg/cm2. The reaction was carried out with stirring for 8 hours at 180° C. After completion of the reaction, the reaction mixture was cooled to room temperature and water was added. The aqueous layer was separated and then acid was added thereto, followed by extraction from the aqueous layer with ether. The ether layer was dried and then concentrated to obtain 101 g of paratrifluoromethylbenzoic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05194631 |
|---|
| Source dataset | uspto-grants-1993_03 |
|---|
| ORD ID | ord-7e26addbca144f9293f7dea343edc70d |
|---|
| Source note | uspto-grants-1993_03 |
|---|