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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 447791생성일: 2026년 10월 24일

Dichloromethane → 1-(Oxan-4-yl)piperidin-4-amine dihydrochloride

https://huagongshe.com/ko/reaction/447791

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Potassium CarbonateHCID 11430—
반응물Tetrahydro-4H-pyran-4-oneHCID 121599—
반응물4-(N-Boc-amino)piperidineHCID 723833—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매WaterHCID 962—
용매Sodium chloride; waterHCID 57417360—
생성물1-(Oxan-4-yl)piperidin-4-amine dihydrochlorideHCID 45156751—

반응 조건

온도0 °C

반응 단계

To a solution of 1,1-dimethylethyl 4-piperidinylcarbamate (50 g) was added tetrahydro-4H-pyran-4-one (35.75 g) in dry DCM (1000 ml), then was added sodium triacetoxyborohydride (141 g) portion wise over 10 minutes at about 25° C. The mixture was stirred under nitrogen for about 30 hours, then cooled to 0° C. Water (107 ml) was added portion wise in 20 minutes, followed by saturated aqueous potassium carbonate (178 ml) and saturated brine (178 g in 178 ml). The mixture was stirred for 10 minutes at about 25° C., then the layers were separated and the organic layer washed with saturated brine (3×214 ml). After drying over anhydrous sodium sulphate, the organic layer was concentrated and the residue was treated with 100 ml isopropanol and reconcentrated. The residue was slowly heated to reflux with 11% HCl in isopropanol (200 ml) for 2 hours then cooled to about 25° C. The solid was filtered, and slurry washed with diethyl ether (100 ml), then dried under high vacuum to give the title product (43 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08481566B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-5535cb3c210d43fa9ee7ebd3c3e33089
출처 메모uspto-grants-2013_07