Acetic Anhydride → alpha-(2-Acetoxy-5-sulfophenylazo)acetoacetanilide

HRID 2052199노트

반응식

HRID 2052199 반응식
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([OH:11])(=[O:10])=[O:9])=[CH:4][C:3]=1[N:12]=[N:13][CH:14]([C:24]([CH3:26])=[O:25])[C:15]([NH:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)=[O:16].[C:27](OC(=O)C)(=[O:29])[CH3:28]>N1C=CC=CC=1>[C:27]([O:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([OH:11])(=[O:10])=[O:9])=[CH:4][C:3]=1[N:12]=[N:13][CH:14]([C:24]([CH3:26])=[O:25])[C:15]([NH:17][C:18]1[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=1)=[O:16])(=[O:29])[CH3:28]

참가 물질

4

반응물 2

HCID 7918Acetic AnhydrideHCID 135839437alpha-(2-Hydroxy-5-sulfophenylazo)acetoacetanilide

생성물 1

HCID 23336111alpha-(2-Acetoxy-5-sulfophenylazo)acetoacetanilide

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

α-(2-hydroxy-5-sulfophenylazo)acetoacetanilide (40 g) was dissolved in boiling pyridine (750 ml) and acetic anhydride (100 ml) added. Some material precipitated while the reaction mixture was hot. After being cooled, the product was filtered off and dried. Yield: 38 g.

후처리

  1. additionadded
  2. customSome material precipitated while the reaction mixture
  3. temperatureAfter being cooled
  4. filtrationthe product was filtered off
  5. customdried

출처 및 근거

ORD 기록
ord-dc614a1fcf76419a9bcd9dce6a459e38
출처 데이터셋
uspto-grants-1980_01
특허 번호
US04183755

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