HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005484Generated: October 30, 2026
Carbon Dioxide → 3-Chloro-2-fluoro-6-(trifluoromethyl)benzoic acid
https://huagongshe.com/reaction/1005484
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 4-Chloro-3-fluorobenzotrifluoride | HCID 2736545 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Chloro-2-fluoro-6-(trifluoromethyl)benzoic acid | HCID 2773754 | 94% |
Reaction Steps
77.0 g of 3-fluoro-4-chlorobenzotrifluoride was dissolved in 750 ml of dried tetrahydrofuran, and to the solution, 250 ml of hexane solution of n-butyl lithium (1.6 mol/l) was added dropwise over 15 minutes at -78° C. under a nitrogen atmosphere. After stirring the solution at -78° C. for 2 hours. 50 g of dry ice was gradually added to the solution at the same temperature. After elevating the temperature of the solution up to room temperature, 500 ml of ice water was added to the solution to separate the resulting solution. While cooling down the aqueous layer, the layer was adjusted to a pH value of 1 with concentrated hydrochloric acid. The aqueous layer was then extracted with ether, washed with water and dried over anhydrous magnesium sulfate. The solvent was distilled under reduced pressure, and the oily residue obtained was crystalized with n-hexane, followed by a filtration and then dried to obtain 88.4 g of the title compound(mp. 92-93° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06054605 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-8b85ed6de7204fdd82bd1c047d044d6c |
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| Source note | uspto-grants-2000_04 |
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