HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 645301Generated: October 25, 2026
Ethyl Acetate → 4-(3-(3,5-Dichlorophenyl)-4,4,4-trifluoro-2-butenoyl)-N-(2-pyridylmethyl)benzoic acid amide
https://huagongshe.com/reaction/645301
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2-Pyridinemethanamine | HCID 19509 | — |
| Reactant | 4-(3-(3,5-Dichlorophenyl)-4,4,4-trifluoro-2-butenoyl)benzoic acid | HCID 66735658 | — |
| Reactant | 1-(3-(Diethylamino)propyl)-3-ethylcarbodiimide chloride | HCID 86626428 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(3-(3,5-Dichlorophenyl)-4,4,4-trifluoro-2-butenoyl)-N-(2-pyridylmethyl)benzoic acid amide | HCID 66735361 | 27.6% |
Reaction Steps
To a solution of 0.5 g of 4-(3-(3,5-dichlorophenyl)-4,4,4-trifluoro-2-butenoyl)benzoic acid that was synthesized under Synthetic Example 4 and 0.21 g of 2-picolylamine in 6 mL of N,N-dimethylformamide, 0.32 g of 1-(3-(diethylamino)propyl)-3-ethylcarbodiimide chloride was added at room temperature and the mixture was stirred for 72 hours. After the completion of reaction, 20 mL of ethyl acetate and 15 mL of saturated saline were added to the reaction solution, the mixture was separated to extract an aqueous layer with 10 mL of ethyl acetate whereto an organic layer was added, the resulting mixture was washed with 10 mL of water and dried with anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. After purification of the resulting residue using silica gel column chromatography that was eluted with ethyl acetate-hexane (5:1) to obtain 0.17 g of aimed product as resinous matter.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700808B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-6fdbcdd4e796477d9300a9ac0b405854 |
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| Source note | uspto-grants-2010_04 |
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