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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 550788생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/550788

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl MalonateHCID 7761—
반응물Ethanol sodium ethoxideHCID 23706232—
반응물1-Tert-butoxycarbonylpiperidin-4-yl benzenesulfonateHCID 86619135—
용매EthanolHCID 702—
생성물Diethyl 2-(1-(tert-butoxycarbonyl)piperidin-4-yl)malonateHCID 59605280—

반응 단계

A mixture of 1-tert-butoxycarbonylpiperidin-4-ol, triethylamine, benzenesulfonyl chloride, and methylene chloride was stirred at ambient temperature for 2 days to yield 1-tert-butoxycarbonylpiperidin-4-yl benzenesulfonate. A mixture of 1-tert-butoxycarbonylpiperidin-4-yl benzenesulfonate obtained, diethyl malonate, 20% NaOEt-EtOH, and EtOH was heated under reflux with stirring for 22 hours to yield diethyl[1-(tert-butoxycarbonyl)piperidin-4-yl]malonate. A mixture of diethyl [1-(tert-butoxycarbonyl)piperidin-4-yl]malonate obtained, lithium borohydride, toluene, and THF was stirred at 60° C. for 18 hours to yield 2-(1-tert-butoxycarbonylpiperidin-4-yl)propane-1,3-diol, which was stirred together with 4M HCl-dioxane solution in MeOH at ambient temperature for 1 hour to yield 2-piperidin-4-ylpropane-1,3-diol hydrochloride.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07947690B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-2ea39f6b43514390b30e9904b0204f6a
출처 메모uspto-grants-2011_05