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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 270604생성일: 2026년 10월 24일

Water → (1S,4S)-4-[(tert-Butoxycarbonyl)amino]-1-(2-methoxyethyl)cyclopent-2-ene-1-carboxylic acid

https://huagongshe.com/ko/reaction/270604

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참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Lithium hydroxide, monohydrateHCID 168937—
반응물Methyl(1S,4S)-4-[(tert-Butoxycarbonyl)amino]-1-(2-methoxyethyl)cyclopent-2-ene-1-carboxylateHCID 59833587—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물(1S,4S)-4-[(tert-Butoxycarbonyl)amino]-1-(2-methoxyethyl)cyclopent-2-ene-1-carboxylic acidHCID 5983354863.4%

반응 조건

온도80 °C

반응 단계

To a stirred solution of methyl (1S,4S)-4-[(tert-butoxycarbonyl)amino]-1-(2-methoxyethyl)cyclopent-2-ene-1-carboxylate (0.78 g, 2.6 mmol) in tetrahydrofuran (1.5 mL), methanol (15 mL), and water (3.0 mL) was added lithium hydroxide monohydrate (0.55 g, 13 mmol) and the resulting orange mixture was stirred at 80° C. overnight. The solvents were evaporated and the mixture was acidified with 6 N HCl to a pH of about 4. The aqueous was then extracted with methylene chloride three times. The combined organic layers were dried (MgSO4), filtered, and concentrated in vacuo to give the desired product as an oil (0.47 g, 63.2%). LCMS calculated for C14H24NO5: (M+H) 286.2; found 286.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07449467B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-56dda64db6f34be1accc8190572f61a7
출처 메모uspto-grants-2008_11