Hydrochloric Acid → (+/-)-alpha-(3,4-Dichlorophenyl)-2,6-dimethyl-4-nitrobenzeneacetonitrile

HRID 965636

反応式

HRID 965636 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]([CH2:9][C:10]#[N:11])[CH:5]=[CH:6][C:7]=1[Cl:8].[H-].[Na+].CO[C:16]1[C:21]([CH3:22])=[CH:20][C:19]([N+:23]([O-:25])=[O:24])=[CH:18][C:17]=1[CH3:26].Cl>CN(C=O)C.O>[Cl:1][C:2]1[CH:3]=[C:4]([CH:9]([C:16]2[C:17]([CH3:26])=[CH:18][C:19]([N+:23]([O-:25])=[O:24])=[CH:20][C:21]=2[CH3:22])[C:10]#[N:11])[CH:5]=[CH:6][C:7]=1[Cl:8]

参加物

7

反応条件

温度
0 °C

実験手順

A mixture of (3,4-dichlorophenyl)acetonitrile (0.149 mol) in DMF (100 ml) was stirred at 0° C. under N2 flow. Sodium hydride (0.223 mol) was added portionwise. The mixture was stirred at 0° C. under N2 flow for 1 hour. A mixture of, 2-methoxy-1,3-dimethyl-5-nitrobenzene (0.149 mol) in DMF (100 ml) was added dropwise at 0° C. under N2 flow. The mixture was stirred at RT for 6 hours, then cooled, hydrolized with H2O and with HCl 3N and extracted with EtOAc. The organic layer was separated, washed several times with H2O, dried, filtered and the solvent was evaporated. The residue was crystallized from DIPE. The precipitate was filtered off and dried, yielding 43.4 g (87%) of (±)-α-(3,4-dichlorophenyl)-2,6-dimethyl-4-nitrobenzeneacetonitrile (interm. 48).

後処理

  1. stirringThe mixture was stirred at 0° C. under N2 flow for 1 hour
  2. additionwas added dropwise at 0° C. under N2 flow
  3. stirringThe mixture was stirred at RT for 6 hours
  4. extractionextracted with EtOAc
  5. customThe organic layer was separated
  6. washwashed several times with H2O
  7. customdried
  8. filtrationfiltered
  9. customthe solvent was evaporated
  10. customThe residue was crystallized from DIPE
  11. filtrationThe precipitate was filtered off
  12. customdried

出典と根拠

ORDレコード
ord-d08b914b289c4b42965af605431dc2e3
出典データセット
uspto-grants-2005_10
特許番号
US06951857B2

関連ノート

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