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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 225767생성일: 2026년 10월 26일

Acetic Acid → Ammonia

https://huagongshe.com/reaction/225767

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물AcetoneHCID 180—
반응물Piperidin-4-olHCID 79341—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매TetrahydrofuranHCID 8028—
생성물AmmoniaHCID 222—
생성물1-Isopropylpiperidin-4-olHCID 79681—

반응 단계

A mixture of 4-hydroxypiperidine (10 g, 0.10 mol), acetone (21.8 mL, 0.30 mol), acetic acid (5.7 mL, 0.10 mol) and tetrahydrofuran (150 mL) was stirred in an ice bath for 15 minutes. Sodium triacetoxyborohydride (31.3 g, 0.15mol) was then added portionwise and the mixture was stirred for a further 10 minutes. The reaction mixture was then warmed and stirred at room temperature for 10 minutes and at 40° C. for 2.5 hours. The solvent was evaporated under reduced pressure and the residue was dissolved in water (50 mL). The aqueous solution was basified to pH9 with 0.88 ammonia and the solution was stirred for 30 minutes. The reaction mixture was then extracted with diethyl ether (2×200 mL) and the combined extracts were dried over sodium sulfate and concentrated in vacuo to give a yellow oil. The oil was purified by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 96:4:1 to 90:10:1, to afford the title product as a yellow oil in quantitative yield, 14.6 g.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07557121B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-b546bb7d2476469faddf9cb39b706090
출처 메모uspto-grants-2009_07