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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 565375생성일: 2026년 10월 24일

(2S,3R)-1-tert-Butoxycarbonyl-3-(3-hydroxypropyn-1-yl)-2-phenylpiperidin-3-ol → Z-(2S,3R)-1-tert-Butoxycarbonyl-3-(3-hydroxyprop-1-en-1-yl)-2-phenylpiperidin-3-ol

https://huagongshe.com/ko/reaction/565375

반응식

참여 물질

역할이름HCID투입량
반응물(2S,3R)-1-tert-Butoxycarbonyl-3-(3-hydroxypropyn-1-yl)-2-phenylpiperidin-3-olHCID 11301992—
촉매PalladiumHCID 23938—
촉매Lindlars catalystHCID 131709914—
용매Ethyl AcetateHCID 8857—
생성물Z-(2S,3R)-1-tert-Butoxycarbonyl-3-(3-hydroxyprop-1-en-1-yl)-2-phenylpiperidin-3-olHCID 59038479100%

반응 단계

Palladium on calcium carbonate, poisoned with lead (Lindlar catalyst, 2 g) was added to a solution of (2S,3R)-1-tert-butoxycarbonyl-3-(3-hydroxypropyn-1yl)-2-phenylpiperidin-3-ol (Description 2; 32 g, 96.6 mmol) in ethyl acetate (300 ml) and the mixture was stirred under hydrogen (1 atmosphere) for 4 hours. The mixture was filtered and the solvent was evaporated under reduced pressure to give the title compound as an oil (32 g, 100%). 1H NMR (360 MHz, CDCl3) δ 7.42 (2H, d, J 7.6 Hz), 7.35−7.25 (3H, m), 5.83 (1H, d, J 12.3 Hz), 5.68 (1H, dt, J 12.3, 6.0 Hz), 5.06 (1H, s), 4.27 (1H, m), 4.12 (2H, m), 3.32 (1H, m), 3.13 (1H, s), 2.28 (1H, t, J 5.9 Hz), 2.02 (1H, m), 1.92−1.78 (3H, m), and 1.32 (9H, s). m/z (ES+) 334 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06172077B2
출처 데이터셋uspto-grants-2001_01
ORD IDord-8015db31df6340149d12302d04bc21c5
출처 메모uspto-grants-2001_01