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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 487457생성일: 2026년 10월 24일

Water → 10-(N-benzyloxycarbonylamino)-2-formylamino-3-hydroxy-4-methylene-decanoic acid ethyl ester

https://huagongshe.com/ko/reaction/487457

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물5-[8-(N-benzyloxycarbonylamino)oct-1-en-2-yl]-oxazoline-4-carboxylic acid ethyl esterHCID 14966608—
용매TetrahydrofuranHCID 8028—
생성물10-(N-benzyloxycarbonylamino)-2-formylamino-3-hydroxy-4-methylene-decanoic acid ethyl esterHCID 14966609—

반응 단계

8.15 g (20.25 mmol) of 5-[8-(N-benzyloxycarbonylamino)oct-1-en-2-yl]-oxazoline-4-carboxylic acid ethyl ester are heated under reflux in 40 ml of tetrahydrofuran and 20 ml of water for 4 hours with stirring. The reaction mixture is concentrated to dryness by evaporation in vacuo at 45°, and the honey-like residue is concentrated by evaporation twice more after the addition of toluene. The crude product is dissolved in dichloromethane, dried with sodium sulfate, filtered and concentrated by evaporation. Drying under a high vacuum at room temperature yields 9.03 g of 10-(N-benzyloxycarbonylamino)-2-formylamino-3-hydroxy-4-methylene-decanoic acid ethyl ester in the form of a yellowish honey.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05294734
출처 데이터셋uspto-grants-1994_03
ORD IDord-f9c6d02cc10e4456bedf8b9288604295
출처 메모uspto-grants-1994_03