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Triethylamine → 2,2,2-Trifluoro-1-(3-nitrophenyl)ethanone oxime

HRID 2307422
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HRID 2307422 반응식
[F:1][C:2]([F:15])([F:14])[C:3]([C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([N+:11]([O-:13])=[O:12])[CH:6]=1)=O.[NH2:16][OH:17].Cl.CCN(CC)CC>CCO>[F:1][C:2]([F:15])([F:14])[C:3]([C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([N+:11]([O-:13])=[O:12])[CH:6]=1)=[N:16][OH:17]
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참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 695662,2,2-Trifluoro-1-(3-nitrophenyl)ethan-1-oneHCID 443297Hydroxyamine hydrochloride

생성물 1

HCID 739856852,2,2-Trifluoro-1-(3-nitrophenyl)ethanone oxime수율 79.5%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of 2,2,2-trifluoro-1-(3-nitro-phenyl)ethanone (4 g), NH2OH.HCl (5.037 g), and Et3N (20.44 g) in EtOH (80 mL) was refluxed for 4 days. After concentration, the residue was extracted with CH2Cl2. The organic layer was washed with water and dried over MgSO4. The crude product was purified by silica gel flash chromatography (30% ethyl acetate in hexanes) to give the title compound (3.4 g) as a solid.

후처리

  1. temperaturewas refluxed for 4 days
  2. concentrationAfter concentration
  3. extractionthe residue was extracted with CH2Cl2
  4. washThe organic layer was washed with water
  5. dry with materialdried over MgSO4
  6. customThe crude product was purified by silica gel flash chromatography (30% ethyl acetate in hexanes)

출처 및 근거

ORD 기록
ord-2278fa11a07f44b9995cb43110b157c1
출처 데이터셋
uspto-grants-2004_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06831080B2

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