HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005480Generated: October 31, 2026
Carbon Dioxide → 2,3-Dichloro-6-(trifluoromethyl)benzoic acid
https://huagongshe.com/reaction/1005480
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 3,4-Dichlorobenzotrifluoride | HCID 9481 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2,3-Dichloro-6-(trifluoromethyl)benzoic acid | HCID 11651803 | 88.6% |
Reaction Steps
83.4 g of 3,4-dichlorobenzotrifluoride was dissolved in 800 ml of dried tetrahydrofuran, and 250 ml of hexane solution of n-butyl lithium(1.6 mol/1) was added to the solution dropwise over 15 minutes at -78° C. under nitrogen atmosphere. Following to stirring the solution for 2 hours at -78° C., 50 g of dry ice was then gradually added to the solution at the same temperature. After elevating the temperature of the solution up to room temperature, 250 ml of cold water was added to the solution to separate the resulting solution, and the aqueous layer obtained was adjusted to an acidic condition of a pH value of 1 with concentrated hydrochloric acid while cooling. Then, the aqueous layer was extracted with ether, and the extract was washed with water and dried over anhydrous magnesium sulfate. The solvent was distilled out under reduced pressure, and the oily residue obtained was crystalized with n-hexane, washed, filtered, and dried to obtain 89 g of the title compound(mp. 88-89° 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-f2d89c5c41894bbe9aa355a5eba760e0 |
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| Source note | uspto-grants-2000_04 |
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