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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 458248생성일: 2026년 10월 23일

4-Chloromandelic acid → 2-(4-Chloro-phenyl)-2-hydroxy-n-(3-methoxy-4-pent-2-ynyloxy-benzyloxy)-acetamide

https://huagongshe.com/ko/reaction/458248

반응식

참여 물질

역할이름HCID투입량
반응물4-Chloromandelic acidHCID 10299—
반응물DiisopropylethylamineHCID 81531—
반응물Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
반응물O-(3-methoxy-4-pent-2-ynyloxy-benzyl)-hydroxylamineHCID 18442094—
용매DimethylformamideHCID 6228—
생성물2-(4-Chloro-phenyl)-2-hydroxy-n-(3-methoxy-4-pent-2-ynyloxy-benzyloxy)-acetamideHCID 18442066—

반응 단계

O-(3-methoxy-4-pent-2-ynyloxy-benzyl)-hydroxylamine (5.0 g, 21 mmol) and N-ethyldiisopropylamine (Hünig's base, 5.5 g, 42 mmol) are dissolved in 60 ml of N,N-dimethylformamide. 4-chloro-DL-mandelic acid (4.1 g, 22 mmol) and (benzotriazol-1-yloxy)-tris-(dimethylamino)-phosphonium hexafluorophosphate (BOP, Castro's reagent, 10 g, 23 mmol) are added successively and the mixture is stirred for 16 h. After pouring the mixture on ice/water, it is extracted with ethyl acetate. The combined organic layer is washed with brine, dried over magnesium sulfate and evaporated under reduced pressure. The remaining oil is purified by chromatography on silica gel (ethyl acetate/hexane (4:6)) to obtain 2-(4-chloro-phenyl)-2-hydroxy-N-(3-methoxy-4-pent-2-ynyloxy-benzyloxy)-acetamide as yellow resin.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07189873B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-921bf4a08a354f3580fa42e39bc8b254
출처 메모uspto-grants-2007_03