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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17793생성일: 2026년 10월 24일

Ethyl (1R,2S)-1-[[(1,1-dimethylethoxy)carbonyl]amino]-2-ethenylcyclopropanecarboxylate → Cyclopropanecarboxylic acid, 1-amino-2-ethenyl-, ethyl ester, hydrochloride (1:1), (1R,2S)-

https://huagongshe.com/ko/reaction/17793

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl (1R,2S)-1-[[(1,1-dimethylethoxy)carbonyl]amino]-2-ethenylcyclopropanecarboxylateHCID 10658673—
반응물1,4-Dioxane hydrochlorideHCID 20443148—
생성물Cyclopropanecarboxylic acid, 1-amino-2-ethenyl-, ethyl ester, hydrochloride (1:1), (1R,2S)-HCID 66670028—

반응 단계

Ethyl 1(R)-tert-butoxycarbonylamino-2(S)-vinylcyclopropanecarboxylate (8.5 g, 33.3 mmol) was stirred under an N2 atmosphere with 200 mL of 4N HCl/dioxane (Aldrich) at rt for 3 h. The solvent was removed under reduced pressure keeping the temperature below 40 C. This gave 6.57 g (˜100%) of ethyl 1(R)-amino-2(S)-vinylcyclopropanecarboxylate hydrochloride as a light tan solid. 1H NMR (300 MHz, CD3OD) δ 1.31 (t, J=7.0 Hz, 3H), 1.69-1.82 (m, 2H), 2.38 (q, J=8.8 Hz, 1H), 4.29 (q, J=7.0 Hz, 2H), 5.22 (d, J=10.3 Hz, 1H), 5.40 (d, J=17.2 Hz, 1H), 5.69-5.81 (m, 1H). MS m/z 156 (M++1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741281B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-2bc0ad80843640a581c0428a955163b5
출처 메모uspto-grants-2010_06