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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 349302생성일: 2026년 10월 25일

Methanol → 7-[2-((E)-3-Hydroxy-oct-1-enyl)-6-oxo-piperidin-1-yl]-heptanoic acid methyl ester

https://huagongshe.com/reaction/349302

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Sodium borohydrideHCID 4311764—
반응물7-[2-Oxo-6-((E)-3-oxo-oct-1-enyl)-piperidin-1-yl]-heptanoic acid methyl esterHCID 10384243—
용매DichloromethaneHCID 6344—
생성물7-[2-((E)-3-Hydroxy-oct-1-enyl)-6-oxo-piperidin-1-yl]-heptanoic acid methyl esterHCID 1031691799%

반응 단계

Sodium borohydride (42 mg, 1.10 mmol), followed by MeOH (0.38 mL), was added to a solution of 7-[2-oxo-6-((E)-3-oxo-oct-1-enyl)-piperidin-1-yl]-heptanoic acid methyl ester (40 mg, 0.11 mmol) in CH2Cl2 (1.13 mL) at 0° C. The mixture was allowed to warm to rt. After 3 h at rt, the reaction was quenched with aqueous HCl (1.0M) and extracted with EtOAc (3×10 mL). The combined organic phase was washed with brine (20 mL) then dried (Na2SO4), filtered and concentrated in vacuo to afford 40 mg (99%) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07179820B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-7e8a99f5aaa14b4f86f5c1bf9ec2d237
출처 메모uspto-grants-2007_02