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

HRID 55457
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인쇄 미리보기

반응식

HRID 55457 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]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

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.

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

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-26f9d88d33cc4916a5ce56fe1bb398c6
출처 데이터셋
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05625059

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