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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10349생성일: 2026년 10월 24일

Ethyl Acetate → 3-(1-Aminoethyl)-3-hydroxypyrrolidine-1-carboxylic acid benzyl ester

https://huagongshe.com/ko/reaction/10349

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Ammonium HydroxideHCID 14923—
반응물Benzyl 2-methyl-1-oxa-5-azaspiro[2.4]heptane-5-carboxylateHCID 21041146—
용매MethanolHCID 887—
생성물3-(1-Aminoethyl)-3-hydroxypyrrolidine-1-carboxylic acid benzyl esterHCID 69068640—

반응 단계

A solution of 2-methyl-1-oxa-5-azaspiro[2,4]heptane-5-carboxylic acid benzyl ester (Example A9, 0.31 g, 1.25 mmol) in methanol (10 mL) and ammonium hydroxide (7 mL) is heated in a sealed tube at 100° C. for 16 hours. After cooling, the reaction mixture is dissolved ethyl acetate, washed with water, dried over Na2SO4 and evaporated to afford the title compound (0.340 g). 1H NMR (200 MHz, CDCl3): δ 7.33–7.26 (m, 5H), 5.28 (bs, 2H), 5.07 (s, 2H), 3.56–3.16 (m, 5H), 2.03–1.76 (m, 2H), 1.15 (d, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094780B1
출처 데이터셋uspto-grants-2006_08
ORD IDord-25d841ff62cf41b6862babb19ab9536f
출처 메모uspto-grants-2006_08