Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 52096생성일: 2026년 10월 25일
Acetic Anhydride → N-[3-(4-Piperidinomethyl-2-pyridyloxy)propyl]-2-(2-acetoxyethylthio)acetamide
https://huagongshe.com/reaction/52096
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Anhydride | HCID 7918 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | N-[3-(4-Piperidinomethyl-2-pyridyloxy)propyl]-2-(2-hydroxyethylthio)acetamide | HCID 19962907 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | N-[3-(4-Piperidinomethyl-2-pyridyloxy)propyl]-2-(2-acetoxyethylthio)acetamide | HCID 19962905 | 75% |
반응 단계
0.49 g of N-[3-(4-piperidinomethyl-2-pyridyloxy)propyl]-2-(2-hydroxyethylthio)acetamide [prepared as described in step (b) above] was added to a mixture of 0.48 ml of acetic anhydride and 0.43 ml of pyridine, and the resulting mixture was warmed at 60° C. for 2 hours. At the end of this time, the reaction mixture was poured into ice-water and a saturated aqueous solution of sodium hydrogencarbonate was added to it. The resulting aqueous mixture was extracted with ethyl acetate. The extract was concentrated by evaporation under reduced pressure, and the concentrate was purified by column chromatography through silica gel, using a 1:9 by volume mixture of methanol and ethyl acetate as the eluent, to give 0.41 g (yield 75%) of the title compound as an oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05616579 |
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| 출처 데이터셋 | uspto-grants-1997_04 |
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| ORD ID | ord-528e689e82c741fab85128b6781164cd |
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| 출처 메모 | uspto-grants-1997_04 |
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