HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1598502Generated: November 2, 2026
Carbon Dioxide → 2,6-dichloro-4-(trifluoromethyl)benzoic Acid
https://huagongshe.com/reaction/1598502
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | 4-Bromo-3,5-dichlorobenzotrifluoride | HCID 1268256 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2,6-dichloro-4-(trifluoromethyl)benzoic Acid | HCID 11680460 | 79% |
Reaction Steps
To a mixture of 65.2 ml of n-butyllithium (1.61M in hexane) and 100 ml of anhydrous ether was added dropwise 29.3 g of 4-bromo-3,5-dichlorobenzotrifluoride (3) in 30 ml of anhydrous ether at -78° C., followed by stirring for 20 minutes. Subsequently, 10 g of dry ice crashed into small pieces was added in small portions to the reaction mixture, followed by stirring at room temperature for 1.5 hours. Ice water was added to the reaction mixture, the mixture was thereafter extracted with ether, and the combined extract was subjected to reverse extraction with 10% aqueous sodium carbonate solution. The aqueous layer was acidified with 6N hydrochloric acid, followed by extraction with ethyl acetate, washing with brine and drying over anhydrous magnesium sulfate. Removal of the solvent under reduced pressure gave 20.4 g of the desired product in the form of white crystals (crude yield 79.1%). mp 117°~118° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05739083 |
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| Source dataset | uspto-grants-1998_04 |
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| ORD ID | ord-5bfd789fee5c4572831d447b514d61cb |
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| Source note | uspto-grants-1998_04 |
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