Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 645301생성일: 2026년 10월 25일
Ethyl Acetate → 4-(3-(3,5-Dichlorophenyl)-4,4,4-trifluoro-2-butenoyl)-N-(2-pyridylmethyl)benzoic acid amide
https://huagongshe.com/reaction/645301
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | 2-Pyridinemethanamine | HCID 19509 | — |
| 반응물 | 4-(3-(3,5-Dichlorophenyl)-4,4,4-trifluoro-2-butenoyl)benzoic acid | HCID 66735658 | — |
| 반응물 | 1-(3-(Diethylamino)propyl)-3-ethylcarbodiimide chloride | HCID 86626428 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 4-(3-(3,5-Dichlorophenyl)-4,4,4-trifluoro-2-butenoyl)-N-(2-pyridylmethyl)benzoic acid amide | HCID 66735361 | 27.6% |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07700808B2 |
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| 출처 데이터셋 | uspto-grants-2010_04 |
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| ORD ID | ord-6fdbcdd4e796477d9300a9ac0b405854 |
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| 출처 메모 | uspto-grants-2010_04 |
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