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Toluene → N-[4-Fluoro-2-[(2-methyl-2-propen-1-yl)oxy]phenyl]acetamide

HRID 496226
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HRID 496226 반응식
Cl[CH2:2][C:3]([CH3:5])=[CH2:4].[F:6][C:7]1[CH:8]=[CH:9][C:10]([N+:14]([O-])=O)=[C:11]([OH:13])[CH:12]=1.[C:17](=[O:20])([O-])[O-].[K+].[K+].S(S([O-])=O)([O-])=O.[Na+].[Na+].[C:31]1(C)C=CC=CC=1>S([O-])(O)(=O)=O.C([N+](CCCC)(CCCC)CCCC)CCC.CCO.C1COCC1.O.N1C=CC=CC=1.ClCCl.C(#N)C>[F:6][C:7]1[CH:8]=[CH:9][C:10]([NH:14][C:17](=[O:20])[CH3:31])=[C:11]([O:13][CH2:2][C:3]([CH3:5])=[CH2:4])[CH:12]=1
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참가 물질

11

반응물 5

HCID 1140TolueneHCID 99375-Fluoro-2-nitrophenolHCID 112413-Chloro-2-methyl-1-propeneHCID 11430Potassium Carbonate2회HCID 24489Sodium Dithionite

생성물 1

HCID 22313556N-[4-Fluoro-2-[(2-methyl-2-propen-1-yl)oxy]phenyl]acetamide

시약·촉매·용매 5

HCID 94433Tetrabutylammonium hydrogen sulfate촉매
HCID 1049Pyridine용매
HCID 6342Acetonitrile용매
HCID 6344Dichloromethane용매
HCID 18504229Ethanol tetrahydrofuran water용매

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온도
50 °C

실험 절차

3-Chloro-2-methylpropene (1.36 g, 15 mmol) was added to a mixture of 5-fluoro-2-nitro-phenol (1.57 g, 10 mmol), potassium carbonate (2.76 g, 20 mmol), tetrabutylammonium hydrogen sulfate (0.068 g, 0.2 mmol) and acetonitrile (30 ml), and the mixture was heated under reflux for 18 h. The cold reaction mixture was diluted with toluene and washed with 5% aqueous potassium carbonate, dried and evaporated. A part of the residue (0.631 g, 3 mmol), sodium dithionite (1.04 g, 6 mmol) in EtOH-THF-H2O (2:1:1, 3 ml) was heated at 75° C. for 4 h. The mixture was portioned between dichloromethane and 15% aqueous potassium carbonate and the organic solution dried and concentrated. The obtained residue was diluted with methanol (1.5 ml) and reacted with acetic anhydride (1.5 ml) at 50° C. for 2 min and allowed to attend room temperature during 20 min, then pyridine (4 ml) was added and the solution heated again at 50° C. for 3 min, cold and concentrated. The material was purified by silica gel chromatography (light petroleum-ethyl acetate 2:1) to give 95 mg of the subtitle compound.

후처리

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 18 h
  3. customThe cold reaction mixture
  4. washwashed with 5% aqueous potassium carbonate
  5. customdried
  6. customevaporated
  7. customthe organic solution dried
  8. concentrationconcentrated
  9. additionThe obtained residue was diluted with methanol (1.5 ml)
  10. customreacted with acetic anhydride (1.5 ml) at 50° C. for 2 min
  11. concentrationcold and concentrated
  12. customThe material was purified by silica gel chromatography (light petroleum-ethyl acetate 2:1)

출처 및 근거

ORD 기록
ord-f56c9bf37723420f8220a0fdf5c055f4
출처 데이터셋
uspto-grants-2005_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06943188B2

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