Pyrrolidine → E-1-(1-pyrrolidinyl)-2-[2-nitro-4-(4-fluorophenoxy)phenyl]ethylene

HRID 263437

反応式

HRID 263437 の反応式
[N+:1]([C:4]1[CH:9]=[C:8]([O:10][C:11]2[CH:16]=[CH:15][C:14]([F:17])=[CH:13][CH:12]=2)[CH:7]=[CH:6][C:5]=1[CH3:18])([O-:3])=[O:2].CO[CH:21](OC)[N:22]([CH3:24])[CH3:23].N1CC[CH2:29][CH2:28]1>CN(C)C=O>[N:22]1(/[CH:24]=[CH:18]/[C:5]2[CH:6]=[CH:7][C:8]([O:10][C:11]3[CH:16]=[CH:15][C:14]([F:17])=[CH:13][CH:12]=3)=[CH:9][C:4]=2[N+:1]([O-:3])=[O:2])[CH2:23][CH2:29][CH2:28][CH2:21]1

参加物

5

反応物 3

HCID 31268PyrrolidineHCID 78373Dimethylformamide dimethyl acetalHCID 35376734-(4-Fluorophenoxy)-1-methyl-2-nitrobenzene

生成物 1

HCID 19038053E-1-(1-pyrrolidinyl)-2-[2-nitro-4-(4-fluorophenoxy)phenyl]ethylene収率 103.4%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
110 °C

実験手順

2-Nitro-4-(4-fluorophenoxy)toluene (11.8 g, 47.7 mmol), was dissolved in dimethylformamide (90.0 mL) under N2 atmosphere. Dimethylformamide dimethyl acetal (20.2 mL, 143 mmol), and pyrrolidine (4.0 mL, 47.4 mmol) were added via syringe and the reaction mixture was heated at 110° C. for 3 hours. The reaction mixture was cooled to ambient temperature and partitioned between H2O and ether. The organic phase was washed with H2O. The combined aqueous extracts were washed with ether. The ether extracts were combined and dried over Na2SO4, filtered, and concentrated in vacuo to give a viscous oil (16.1 g) which was used without further purification.

後処理

  1. temperatureThe reaction mixture was cooled to ambient temperature
  2. custompartitioned between H2O and ether
  3. washThe organic phase was washed with H2O
  4. washThe combined aqueous extracts were washed with ether
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-91ad2b0cc9b648a99f036c8dce7d451b
出典データセット
uspto-grants-1997_07
特許番号
US05643922

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