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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1945537생성일: 2026년 10월 26일

Sodium borohydride → Diethyl 2-(1-(tert-butoxycarbonyl)piperidin-4-yl)malonate

https://huagongshe.com/reaction/1945537

반응식

참여 물질

역할이름HCID투입량
반응물Sodium borohydrideHCID 4311764—
반응물Diethyl 2-(1-(tert-butoxycarbonyl)piperidin-4-ylidene)malonateHCID 59605837—
생성물Diethyl 2-(1-(tert-butoxycarbonyl)piperidin-4-yl)malonateHCID 5960528085%

반응 단계

To IMS (200 mL) at 0° C., NaBH4 (1.87 g, 0.047 mol) and a solution of 2-(1-(tert-butoxycarbonyl)piperidin-4-ylidene)malonic acid diethyl ester (17 g, 0.050 mol) in IMS (200 mL) were added. The resulting mixture was allowed to warm to ambient temperature and stirred for 1 h, then quenched with water and concentrated in vacuo. The resulting oil was then partitioned between EtOAc and water. The organic layer was separated and washed with brine, then dried (MgSO4) and concentrated in vacuo to afford the title compound as a yellow oil (14.6 g, 85%). LCMS (Method H): RT=3.90 min, [M+Na]+ 366.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08394796B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-a9865f61559241a29699f22d9698ecf0
출처 메모uspto-grants-2013_03