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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 60241생성일: 2026년 10월 24일

Beta-Propiolactone → tert-Butyl 1-(oxetan-3-yl)piperidin-4-yl carbamate

https://huagongshe.com/ko/reaction/60241

반응식

참여 물질

역할이름HCID투입량
반응물Beta-PropiolactoneHCID 2365—
반응물4-(N-Boc-amino)piperidineHCID 723833—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매1,2-DichloroethaneHCID 11—
생성물tert-Butyl 1-(oxetan-3-yl)piperidin-4-yl carbamateHCID 5660452867%

반응 단계

To a suspension of piperidin-4-yl-carbamic acid tert-butyl ester (200 mg, 1.0 mmol) in DCE (6 mL) was added oxetanone (60 mg, 0.83 mmol) in DCE (2 mL). After 75 min, sodium triacetoxyborohydride (282 mg, 1.33 mmol) was added in one portion. After 20 hours at ambient temperature, the reaction mixture was loaded directly onto a 5 g SCX-2 cartridge which was washed with methanol, then 2N ammonia in methanol. Concentration of the combined basic fractions in-vacuo followed by flash chromatography of the resultant residue (silica, 5 g column, Si-SPE, 0-10% methanol in dichloromethane) afforded the title compound as a white solid (141 mg, 67%). 1H NMR (300 MHz, CDCl3): 4.62-4.61 (m, 4H), 4.44 (s, 1H), 3.46-3.45 (m, 2H), 2.67 (d, J=10.9 Hz, 2H), 2.02-1.88 (m, 4H), 1.44 (s, 9H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440976B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-21ed99da9d1943258608cfc03367be3a
출처 메모uspto-grants-2016_09