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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 356982생성일: 2026년 10월 24일

1,5-Diphenylpentan-3-one → 1,5-Diphenylpentan-3-amine

https://huagongshe.com/ko/reaction/356982

반응식

참여 물질

역할이름HCID투입량
반응물1,5-Diphenylpentan-3-oneHCID 21496—
반응물Sodium AcetateHCID 517045—
반응물Ammonium AcetateHCID 517165—
반응물Sodium cyanoborohydrideHCID 5003444—
용매MethanolHCID 887—
생성물1,5-Diphenylpentan-3-amineHCID 15388874—

반응 단계

To a solution of 1,5-Diphenylpentan-3-one (5.26 g, 22.1 mmol), ammonium acetate (8.52 g, 110.5 mmol) and sodium acetate (9.06 g, 110.5 mmol) in methanol (80 mL) was added a solution of sodium cyanoborohydride (1.67 g, 26.52 mmol) in methanol (20 mL) and the reaction heated to reflux. After stirring at reflux for 30 min, the reaction was cooled and concentrated to dryness. The residue was partioned between methylene chloride and 2N sodium hydroxide. The organic phase was separated, washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. Chromatography of the residue on silica gel (elution with 2-5% methanol/methylene chloride) provided N-(1-phenethyl-3-phenyl-propyl)amine. To a solution of the above amine (2.1 g, 8.82 mmol) in ethanol (50 mL), was added 2-imidazole-carboxaldehyde (813 mg, 8.47 mmol) and the reaction heated to 50° C. After stirring for 2 hr, the resulting homogeneous solution was treated with sodium borohydride (400 mg, 10.58 mmol) and allowed to stir overnight. The reaction was concentrated to dryness and the residue was partioned between methylene chloride and 2N sodium hydroxide. The organic phase was separated, washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. Chromatography of the residue on silica gel (elution with 5% methanol/methylene chloride) provided compound 22.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05840736
출처 데이터셋uspto-grants-1998_11
ORD IDord-8e5db99a58c8417c9d8a0ab6b4b49e95
출처 메모uspto-grants-1998_11