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Acetic Anhydride → N-(3-fluoro-2-formyl-phenyl)-acetamide

HRID 1294566
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인쇄 미리보기

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HRID 1294566 반응식
[NH2:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([F:10])[C:3]=1[CH:4]=[O:5].[C:11](OC(=O)C)(=[O:13])[CH3:12].C([O-])([O-])=O.[Na+].[Na+]>O>[F:10][C:6]1[C:3]([CH:4]=[O:5])=[C:2]([NH:1][C:11](=[O:13])[CH3:12])[CH:9]=[CH:8][CH:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7918Acetic AnhydrideHCID 10340Sodium CarbonateHCID 217194752-Amino-6-fluorobenzaldehyde

생성물 1

HCID 23106215N-(3-fluoro-2-formyl-phenyl)-acetamide

시약·촉매·용매 1

HCID 962Water용매

반응 조건

온도
70 °C

실험 절차

1.37 g (9.85 mmol) 2-amino-6-fluoro-benzaldehyde are combined with 20 ml acetic anhydride and heated to 70° C. for 4 h. Then the reaction mixture is stirred into 200 ml dist. water, adjusted to pH 7 with Na2CO3 and extracted three times with 50 ml of ethyl acetate. Then the organic phase is dried with MgSO4, the solvent is eliminated in vacuo. The crude product is purified by column chromatography. The carrier material used is silica gel and the eluant used is a mixture of cyclohexane:ethyl acetate (80:20).

후처리

  1. extractionextracted three times with 50 ml of ethyl acetate
  2. dry with materialThen the organic phase is dried with MgSO4
  3. customThe crude product is purified by column chromatography
  4. additiona mixture of cyclohexane:ethyl acetate (80:20)

출처 및 근거

ORD 기록
ord-e14bf518de48403ea3cdb852d790be81
출처 데이터셋
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07241769B2

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