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Acetic Anhydride → Methyl 2-acetoxy-5-benzylideneaminobenzoate

HRID 2107010
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인쇄 미리보기

반응식

HRID 2107010 반응식
[OH:1][C:2]1[CH:11]=[CH:10][C:9]([N:12]=[CH:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5].[C:20](OC(=O)C)(=[O:22])[CH3:21]>N1C=CC=CC=1>[C:20]([O:1][C:2]1[CH:11]=[CH:10][C:9]([N:12]=[CH:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5])(=[O:22])[CH3:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7918Acetic AnhydrideHCID 23047222Methyl 2-hydroxy-5-benzylideneaminobenzoate

생성물 1

HCID 23047224Methyl 2-acetoxy-5-benzylideneaminobenzoate수율 49%

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

Methyl 2-hydroxy-5-benzylideneaminobenzoate (23.5 g, 92.2 mmole) was dissolved in pyridine (50 ml) and acetic anhydride (11 ml) was added after which the reaction mixture was left at room temperature for 48 hours and evaporated to dryness, in vacuo. The remaining material was recrystallized from hexane to give the title compound (13.4 g, 49%), m.p. 101°-103° C. Found (Calc. for C17H15NO4) C 68.57 (68.69), H 4.98 (5.05) N 4.80 (4.71).

후처리

  1. customevaporated to dryness, in vacuo
  2. customThe remaining material was recrystallized from hexane

출처 및 근거

ORD 기록
ord-1c4b1bb63d874561a6db322f52de952c
출처 데이터셋
uspto-grants-1990_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04933330

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