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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 517669생성일: 2026년 10월 26일

Sulfuric Acid → (2S)-5-[(benzyloxy)amino]-2-cyanopiperidine

https://huagongshe.com/reaction/517669

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물Potassium BicarbonateHCID 516893—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물(2S)-5-[(benzyloxy)imino]-2-cyanopiperidineHCID 90088575—
용매Ethyl AcetateHCID 8857—
생성물(2S)-5-[(benzyloxy)amino]-2-cyanopiperidineHCID 11759934588%

반응 조건

온도25 °C

반응 단계

Sulphuric acid (11.7 ml, 0.217 mol) was slowly added to a stirred solution of (2S)-5-[(benzyloxy)imino]-2-cyanopiperidine (IX) (10 gm, 0.0436 mol, prepared according to the procedure described in step 6) in ethyl acetate (150 ml) at −10° C. After 10 minutes of stirring, sodium triacetoxy borohydride (NaHB(OOCCH3)3) (11.7 gm, 0.0519 mol, 95% purity) was added in small portions while maintaining temperature below −5° C. After completion of the addition, stirring was further continued for 2 hour at the same temperature. The pH of the reaction mixture was adjusted to about pH 7 by using 30% aqueous potassium hydrogen carbonate solution. The mixture was allowed to warm to 25° C. and the reaction mixture was filtered under suction. The organic layer was separated and the aqueous layer extracted with fresh ethyl acetate (50 ml). The combined organic layer was washed with water (50 ml) and brine (50 ml), dried over anhydrous sodium sulphate and the solvent evaporated under reduced pressure to obtain 8.88 gm of (2S)-5-[(benzyloxy)amino]-2-cyanopiperidine (X) as an oil, in 88% yield. This was used as such for the next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09115131B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-11cd144b00c34a06b286f049aa7d3018
출처 메모uspto-grants-2015_08