HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973788Generated: October 30, 2026
Triethylamine → 2-(2,4-Difluoroanilino)-4,5-difluorobenzoic acid
https://huagongshe.com/reaction/973788
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,4-Difluoroaniline | HCID 9709 | — |
| Reactant | 2-Chloro-4,5-difluorobenzoic acid | HCID 737171 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(2,4-Difluoroanilino)-4,5-difluorobenzoic acid | HCID 14997475 | 63.1% |
Reaction Steps
A suspension of triethyl amine (15 ml, 0.11 mol), 2, 4-difluoroaniline (25 ml, 0.24 mol), copper bronze (2.7 g., 0.04 mol), in hot DMF (25 ml) was treated with a solution of 2-chloro-4,5-difluorobenzoic acid (23 g., 0.12 mol) in 25 ml of DMF and the temperature was maintained at 85° C. for 8 hours. The reaction mixture was allowed to cool to room temperature and was then stirred overnight. The reaction mixture was evaporated in vacuo and the residue was partitioned between ether and aqueous ammonium chloride. The organic phase was washed with 2N HCl and saturated aqueous lithium chloride solution. The ether was dried over sodium sulfate, treated with darco and then filtered and evaporated. The residue was crystallized from hexane-ether to afford 21.6 g (62%) of 2-(2,4-difluorophenylamino)-4,5-difluorobenzoic acid; m.p.: 215°-216° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05064958 |
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| Source dataset | uspto-grants-1991_11 |
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| ORD ID | ord-ff785fd0d63b490992f893eb0cd5360c |
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| Source note | uspto-grants-1991_11 |
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