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AcOH AcOAc → N-(3-Cyano-4-(ethylsulfonyl)phenyl)acetamide

HRID 1667587
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HRID 1667587 반응식
[CH2:1]([S:3]([C:6]1[CH:13]=[CH:12][C:11]([N+:14]([O-])=O)=[CH:10][C:7]=1[C:8]#[N:9])(=[O:5])=[O:4])[CH3:2].[C:17](O)(=[O:19])[CH3:18].C(OC(=O)C)(=O)C>[Fe]>[C:8]([C:7]1[CH:10]=[C:11]([NH:14][C:17](=[O:19])[CH3:18])[CH:12]=[CH:13][C:6]=1[S:3]([CH2:1][CH3:2])(=[O:5])=[O:4])#[N:9]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 21895370AcOH AcOAcHCID 574481822-Ethylsulfonyl-5-nitrobenzonitrile

생성물 1

HCID 57448183N-(3-Cyano-4-(ethylsulfonyl)phenyl)acetamide수율 83%

시약·촉매·용매 1

HCID 23925Iron촉매

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온도
100 °C

실험 절차

To 5B (3.60 g, 15.0 mmol) in 1:1 acetic acid/acetic anhydride (150 mL), Fe (4.20 g, 75.2 mmol) was added. The reaction mixture was heated to 100° C. for 2 h then poured into ice. After the ice melted, the product was extracted with ethyl acetate, and the organic layer was washed with saturated aqueous NaHCO3 and brine. The organic layer was dried (Na2SO4), filtered and concentrated to provide 5C (3.14 g, 83%). LC-MS: 241.18 (M+H)+.

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후처리

  1. additionthen poured into ice
  2. extractionthe product was extracted with ethyl acetate
  3. washthe organic layer was washed with saturated aqueous NaHCO3 and brine
  4. dry with materialThe organic layer was dried (Na2SO4)
  5. filtrationfiltered
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-0cbc4430504741bbaca3cef9e5e9c921
출처 데이터셋
uspto-grants-2011_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08044242B2

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