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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

반응식

참여 물질

역할이름HCID투입량
반응물4-ButyloxyanilineHCID 20352—
반응물Phosphorus oxychlorideHCID 24813—
반응물Sodium BicarbonateHCID 516892—
반응물(1-Benzyl-4-hydroxypiperidin-4-yl) acetic acid lithium saltHCID 69894340—
용매PyridineHCID 1049—
용매DichloromethaneHCID 6344—
생성물N-(4-n-butoxyphenyl)-2-(1-benzyl-4-hydroxypiperidin-4-yl)acetamideHCID 1782386524%

반응 조건

온도7.5 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710060B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-23334740640f45f081f14beef34c204b
출처 메모uspto-grants-2004_03