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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 242659생성일: 2026년 10월 26일

Acetaldehyde → Tert-butyl 3-(ethylamino)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/242659

반응식

참여 물질

역할이름HCID투입량
반응물AcetaldehydeHCID 177—
반응물(R)-(+)-1-Boc-3-aminopyrrolidineHCID 854070—
반응물Sodium borohydrideHCID 4311764—
용매MethanolHCID 887—
생성물Tert-butyl 3-(ethylamino)pyrrolidine-1-carboxylateHCID 20800658—

반응 조건

온도80 °C

반응 단계

To a solution of (R)-3-amino-1-N-Boc pyrrolidine (1 eq, 5.37 mmol) in methanol (20 mL) was added acetaldehyde (0.95 eq) and the resulting mixture was heated to 80° C. and stirred for 2 h., then stirred at room temperature overnight. Sodium borohydride (0.95 eq, 5.1 mmol) was added and reaction mixture was stirred for an additional 2 h. The reaction mixture was concentrated, dissolved in ethyl acetate and washed with saturated aqueous sodium bicarbonate. The combined organics were washed with brine and dried over sodium sulfate. The crude product was purified on silica using hexane/ethyl acetate (10%) to hexane/ethyl acetate (50%). 1H-NMR (CDCL3) δ: 1.05 (3H, t), 1.45 (9H, s), 1.60-1.75 (1H, m), 2.00-2.10 (1H, m), 2.68 (4H, q), 2.90-3.15 (1H, m), 3.25-3.65 (4H, m). ESI-MS m/z: 215 (M+1), UV retention time: 0.75 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653096B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-6de36c0f01444b1d873210d6f2fcf513
출처 메모uspto-grants-2014_02