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2-Methylbenzenesulfonic acid hydrate → (R)-2-acetamido-3-ethoxycarbonyl-2-penten-4-olide

HRID 1033838
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인쇄 미리보기

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HRID 1033838 반응식
[NH2:1][C:2]1[C:3]([O:5][C@H:6]([CH3:13])[C:7]=1[C:8]([O:10][CH2:11][CH3:12])=[O:9])=[O:4].[OH2:14].[C:15]1([CH3:25])C(S(O)(=O)=O)=CC=CC=1>C(OC(=O)C)(=O)C>[C:15]([NH:1][C:2]1[C:3]([O:5][C@H:6]([CH3:13])[C:7]=1[C:8]([O:10][CH2:11][CH3:12])=[O:9])=[O:4])(=[O:14])[CH3:25]
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참가 물질

4

반응물 2

HCID 124969952-Methylbenzenesulfonic acid hydrateHCID 22851708(R)-2-amino-3-ethoxycarbonyl-2-penten-4-olide

생성물 1

HCID 22851706(R)-2-acetamido-3-ethoxycarbonyl-2-penten-4-olide

시약·촉매·용매 1

HCID 7918Acetic Anhydride용매

반응 조건

온도
40 °C

실험 절차

12.04 g of (R)-2-amino-3-ethoxycarbonyl-2-penten-4-olide are dissolved in 48 ml of acetic anhydride, 125 mg of toluenesulphonic acid monohydrate are added and the whole is stirred overnight at 40° C. The mixture is concentrated by evaporation, dissolved in ethyl acetate and washed with water. The ethyl acetate is distilled off and the residue is recrystallised from ethyl acetate/cyclohexane, [α]D20 =+62.3° (3% in CHCl3), m.p. 119°-122° C.

후처리

  1. concentrationThe mixture is concentrated by evaporation
  2. dissolutiondissolved in ethyl acetate
  3. washwashed with water
  4. distillationThe ethyl acetate is distilled off
  5. customthe residue is recrystallised from ethyl acetate/cyclohexane, [α]D20 =+62.3° (3% in CHCl3), m.p. 119°-122° C.

출처 및 근거

ORD 기록
ord-523f0648441e4a9ab422680dbd6ca173
출처 데이터셋
uspto-grants-1994_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05312914

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