Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49961생성일: 2026년 10월 25일
4-Butyloxyaniline → N-(4-n-butoxyphenyl)-2-(1-benzyl-4-hydroxypiperidin-4-yl)acetamide
https://huagongshe.com/reaction/49961
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Butyloxyaniline | HCID 20352 | — |
| 반응물 | Phosphorus oxychloride | HCID 24813 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | (1-Benzyl-4-hydroxypiperidin-4-yl) acetic acid lithium salt | HCID 69894340 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-(4-n-butoxyphenyl)-2-(1-benzyl-4-hydroxypiperidin-4-yl)acetamide | HCID 17823865 | 24% |
반응 단계
To a solution of (1-benzyl-4-hydroxypiperidin-4-yl) acetic acid lithium salt (3.09 g) in methylene chloride (60 mL) were added 4-n-butoxyaniline (2.0 g) and pyridine (2.14 mL). Phosphorous oxychloride (1.19 mL) was added dropwise to the solution under cooling with an ice-sodium chloride, followed by stirring at 5 to 10° C. for 1 hour. The mixture was made alkaline with saturated aqueous sodium bicarbonate under cooling with an ice-water, and the solution was extracted with ethyl acetate. The organic layer was washed with water and saturated brine and dried over anhydrous sodium sulfate, and then, the solvent was distilled off under reduced pressure. The residue was purified with silica gel column chromatography (elution solvent; methylene chloride:methanol=19:1 to 9:1) to obtain the titled compound (1.15 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06710060B2 |
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| 출처 데이터셋 | uspto-grants-2004_03 |
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| ORD ID | ord-23334740640f45f081f14beef34c204b |
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| 출처 메모 | uspto-grants-2004_03 |
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