Diethyl Ether → HCID 20375614、化合物

HRID 1833378ノート

反応式

HRID 1833378 の反応式
[H-].[Na+].[Cl:3][C:4]1[CH:22]=[CH:21][C:7]([CH2:8][N:9]2[C:18]3[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=3)[C:12]([CH3:19])=[CH:11][C:10]2=[O:20])=[CH:6][CH:5]=1.[C:23](OCC)(=[O:29])[C:24]([O:26][CH2:27][CH3:28])=[O:25].CCOCC>CN(C)C=O>[Cl:3][C:4]1[CH:5]=[CH:6][C:7]([CH2:8][N:9]2[C:18]3[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=3)[C:12]([CH2:19][C:23](=[O:29])[C:24]([O:26][CH2:27][CH3:28])=[O:25])=[CH:11][C:10]2=[O:20])=[CH:21][CH:22]=1

参加物

6

実験手順

Sodium hydride (18g.; 60% w/w dispersion in oil, washed as described in Example 1) was stirred in dry dimethylformamide (300 ml.), and 1-(4-chlorobenzyl)-1,2-dihydro-4-methyl-2-oxoquinoline (64.7 g.) was added, followed by diethyl oxalate (55 g.). The mixture was stirred at room temperature for 2.5 hours with occasional external cooling to keep the temperature below 25° C. Ether (2 1.) was added, and the mixture was filtered. The solid residue was washed with ether (500 ml.), and then suspended in dimethylformamide (200ml.) nd acidified to pH 2 by the addition of concentrated hydrochloric acid. The resultant mixture was added to water (3 1.), and the mixture filtered, and the solid residue washed with water (2 1.), drained well, and crystallised from ethanol to give ethyl 1-(4-chlorobenzyl)-1,2-dihydro-2-oxoquinol-4-ylpyruvate, m.p. 180°-182° C.

後処理

  1. temperatureexternal cooling
  2. customthe temperature below 25° C
  3. filtrationthe mixture was filtered
  4. washThe solid residue was washed with ether (500 ml.)
  5. additionacidified to pH 2 by the addition of concentrated hydrochloric acid
  6. additionThe resultant mixture was added to water (3 1.)
  7. filtrationthe mixture filtered
  8. washthe solid residue washed with water (2 1.)
  9. customcrystallised from ethanol

出典と根拠

ORDレコード
ord-0d60a1a47a774717afb8b3523580848f
出典データセット
uspto-grants-1978_01
特許番号
US04066651

反応ノート

読み込み中…