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Acetic Anhydride → 3-Acetyl-5-(3,4-dimethoxyphenyl)-2-oxazolidinone

HRID 2052559
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반응식

HRID 2052559 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:11]2[O:15][C:14](=[O:16])[NH:13][CH2:12]2)[CH:6]=[CH:7][C:8]=1[O:9][CH3:10].[C:17](OC(=O)C)(=[O:19])[CH3:18]>N1C=CC=CC=1>[C:17]([N:13]1[CH2:12][CH:11]([C:5]2[CH:6]=[CH:7][C:8]([O:9][CH3:10])=[C:3]([O:2][CH3:1])[CH:4]=2)[O:15][C:14]1=[O:16])(=[O:19])[CH3:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7918Acetic AnhydrideHCID 30506615-(3,4-Dimethoxyphenyl)-4,5-dihydro-1,3-oxazol-2-ol

생성물 1

HCID 203762173-Acetyl-5-(3,4-dimethoxyphenyl)-2-oxazolidinone수율 73%

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

8.9 mmol of 5-(3,4-dimethoxyphenyl)-2-oxazolidinone is combined with 10 ml. of acetic anhydride and 5 ml. of pyridine and heated for 5 hours to 100°. After concentrating the reaction mixture, it is recrystallized from ethyl acetate, thus obtaining 3-acetyl-5-(3,4-dimethoxyphenyl)-2-oxazolidinone in a 73% yield, m.p. 175°-182°.

후처리

  1. concentrationAfter concentrating the reaction mixture, it
  2. customis recrystallized from ethyl acetate, thus obtaining 3-acetyl-5-(3,4-dimethoxyphenyl)-2-oxazolidinone in a 73% yield, m.p. 175°-182°

출처 및 근거

ORD 기록
ord-97ea86f2edc5482ea8e366bc7dbf8b27
출처 데이터셋
uspto-grants-1980_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04186129

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