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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 503711생성일: 2026년 10월 23일

1-Propanol → Tert-butyl 3-(benzyloxycarbonylamino)-4-hydroxy-pyrrolidine-1-carboxylate

https://huagongshe.com/ko/reaction/503711

반응식

참여 물질

역할이름HCID투입량
반응물1-PropanolHCID 1031—
반응물1,3-Dichloro-5,5-dimethylhydantoinHCID 8360—
반응물Sodium SulfiteHCID 24437—
반응물tert-Butyl 2,5-dihydro-1H-pyrrole-1-carboxylateHCID 5148195—
반응물N-benzylcarbamateHCID 22253685—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
용매Sodium HydroxideHCID 14798—
생성물Tert-butyl 3-(benzyloxycarbonylamino)-4-hydroxy-pyrrolidine-1-carboxylateHCID 20691380—

반응 조건

온도0 °C

반응 단계

N-Propanol (20 ml), benzylcarbamate (4 g, 27 mmol), and 1,3-dichloro-5,5-dimethylhydantoin (2.6 g, 13 mmol) are added to a solution of NaOH (1 g, 27 mmol) in water (40 ml). The reaction mixture is cooled to 0° C. and a solution of 2,5-dihydro-pyrrole-1-carboxylic acid tert-butyl ester (1.51 g, 8.92 mmol) in n-propanol (10 ml) is added. A solution of potassium osmate (0.098 g, 0.268 mmol) in 0.65 M NaOH (1 ml) is added. The reaction mixture is stirred at 0° C. for 1 hour and then at room temperature for 2 hours. The reaction mixture is quenched with sodium sulfite (1.90 g, 15 mmol) and diluted with approximately 1:1 EtOAc:water (100 ml). The aqueous layer is extracted with ethyl acetate, the combined organic extracts dried (MgSO4) and concentrated. Purification on a silica gel column (4:1 hexanes:EtOAc) yields 3-benzyloxycarbonylamino-4-hydroxy-pyrrolidine-1-carboxylic acid tert-butyl ester.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07777032B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-ddaaf293efb845c285160f35a6a0829f
출처 메모uspto-grants-2010_08