HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172694Generated: November 1, 2026
Carbon Dioxide → 4-Cyano-2,6-difluorobenzoic acid
https://huagongshe.com/reaction/2172694
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | 3,5-Difluorobenzonitrile | HCID 587204 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Cyano-2,6-difluorobenzoic acid | HCID 44557933 | 55.6% |
Reaction Steps
To a solution of 3,5-difluorobenzonitrile (3.48 g, 25 mmol, Fluorochem) in THF (35 ml) was added slowly butyl lithium (1.6M in hexanes) (15.63 ml, 25.00 mmol) at −75° C. The resulting solution was stirred for 1 hr at −70-75° C. Then this solution was poured on freshly crushed dry ice CO2 (44.0 g, 1000 mmol). The contents were stirred at room temperature until dry ice disappearance. The solvent was evaporated off under HV. Then residual organic layer was suspended in water and extracted with ethyl acetate (3×50 ml). The product containing aqueous layer was acidified with aqueous HCl solution and the product was re-extracted in the organic layer with Ethylacetate (4×50 ml). The combined organic layers were washed with brine, dried over MgSO4, filtered and evaporated to give a white crystalline solid (2.5731 g, 13.91 mmol, 55.6% yield)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09056843B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-830c65f007d4438a9490a9cd99f9e041 |
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| Source note | uspto-grants-2015_06 |
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