HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 749485Generated: October 26, 2026
Triethylamine → Ethyl 2-[2,4-dichloro-5-(2-chloro-4,6-difluorophenylamino)benzoyl]-3-dimethylaminoacrylate
https://huagongshe.com/reaction/749485
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Ethyl 3-(N,N-dimethylamino)acrylate | HCID 121015 | — |
| Reactant | 2,4-Dichloro-5-(2-chloro-4,6-difluorophenylamino)benzoic acid | HCID 68798267 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl 2-[2,4-dichloro-5-(2-chloro-4,6-difluorophenylamino)benzoyl]-3-dimethylaminoacrylate | HCID 68796206 | 23.3% |
Reaction Steps
95 mg (0.27 mmol) of 2,4-dichloro-5-(2-chloro-4,6-difluorophenylamino)benzoic acid were boiled with 0.98 ml of thionyl chloride under reflux for 3 hours. The thionyl chloride was distilled off, and the residue was mixed with 3 ml of toluene and concentrated in vacuo. The residue was taken up in 2 ml of toluene and added to a solution of 39 mg (0.27 mmol) of ethyl 3-dimethylaminoacrylate, 6 μl of triethylamine and 1 ml of toluene. The mixture was heated at 90° C. for 3 hours. The mixture was concentrated and chromatographed on silica gel (heptane:ethyl acetate=75:25 to 0:100 in 45 minutes). 30 mg (23%) of the desired product were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07402674B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-f63dff0bbe204ed5aa229156fe2f37ea |
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| Source note | uspto-grants-2008_07 |
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