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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 733092생성일: 2026년 10월 24일

Acetic Acid → Methyl 1-[(4-{[(tert-butoxycarbonyl)amino]methyl}piperidin-1-yl)methyl]cyclobutanecarboxylate

https://huagongshe.com/ko/reaction/733092

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Sodium BicarbonateHCID 516892—
반응물Tert-butyl (piperidin-4-ylmethyl)carbamateHCID 723429—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물Methyl 1-formylcyclobutane-1-carboxylateHCID 15656335—
용매TetrahydrofuranHCID 8028—
생성물Methyl 1-[(4-{[(tert-butoxycarbonyl)amino]methyl}piperidin-1-yl)methyl]cyclobutanecarboxylateHCID 6723339183.2%

반응 조건

온도60 °C

반응 단계

To a stirred mixture of tert-butyl(piperidin-4-ylmethyl)carbamate (12.8 g, 60 mmol) and methyl 1-formylcyclobutanecarboxylate (2.13 g, 15 mmol, Davis, Charles R.; Swenson, Dale C.; Burton, Donald J., J. Org. Chem., 1993, 58, 6843) in tetrahydrofuran (50 mL) was added acetic acid (8.6 mL, 150 mmol) at ambient temperature. After 30 min, sodium triacetoxyborohydride (12.7 g, 60 mmol) was added to the mixture. Then, the mixture was heated to 60° C. for 2 h. After cooling, the reaction mixture was poured into sat. NaHCO3 aq. The aqueous layer was extracted with CH2Cl2 for 3 times. The combined organic phase were washed with brine, dried over MgSO4, filtered and concentrated. The residue was chromatographed on a column of silica gel eluting with hexane/ethyl acetate (1:1) to give 4.25 g (83%) of the title compound as white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07589109B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-7d351ffb7d2645e6b188a7254df7a931
출처 메모uspto-grants-2009_09