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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1404497생성일: 2026년 10월 24일

Acetic Acid → tert-Butyl [5-(4-chlorophenyl)-6-methyl-2-oxopiperidin-3-yl]carbamate

https://huagongshe.com/ko/reaction/1404497

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Potassium CarbonateHCID 11430—
반응물Sodium BicarbonateHCID 516892—
반응물Ammonium AcetateHCID 517165—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물Methyl 2-[(tert-butoxycarbonyl)amino]-4-(4-chlorophenyl)-5-oxohexanoateHCID 68747752—
용매EthanolHCID 702—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물tert-Butyl [5-(4-chlorophenyl)-6-methyl-2-oxopiperidin-3-yl]carbamateHCID 86665200—

반응 조건

온도60 °C

반응 단계

To a solution of methyl 2-[(tert-butoxycarbonyl)amino]-4-(4-chlorophenyl)-5-oxohexanoate (21.6 g, 58.4 mmol) in methanol (200 mL) were added ammonium acetate (45.0 g, 584 mmol), acetic acid (50.2 mL, 876 mmol), and sodium cyanoborohydride (5.51 g, 87.7 mmol). The mixture was heated at 60° C. for a total of 4 h. The mixture was then allowed to cool to ambient temperature and sodium bicarbonate and water were added. The mixture was extracted with ethyl acetate (3×). The combined organic extracts were washed with brine, dried over magnesium sulfate, filtered and concentrated. Ethanol (240 mL) and potassium carbonate (40.4 g, 292 mmol) were added. The mixture was stirred 1.5 h at 60° C. to effect epimerization to the desired epimer. Water was added followed by extraction with ethyl acetate (3×). The combined organic extracts were washed with brine, dried over magnesium sulfate, filtered and concentrated. Purification by silica gel chromatography (100% dichloromethane→90% dichloromethane/methanol with 0.1% ammonium hydroxide) gave the title compound as a mixture of isomers. MS: m/z=361.2 (M+Na).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08912210B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-b58d1e6b667d4eadb8c911cbc445f1b4
출처 메모uspto-grants-2014_12