Dimethylformamide → 4-Chloro-8-methoxy-2-(trifluoromethyl)quinoline

HRID 2301433ノート

反応式

HRID 2301433 の反応式
O[C:2]1[C:11]2[C:6](=[C:7]([O:12][CH3:13])[CH:8]=[CH:9][CH:10]=2)[N:5]=[C:4]([C:14]([F:17])([F:16])[F:15])[CH:3]=1.CN(C=O)C.O=P(Cl)(Cl)[Cl:25]>C(Cl)Cl>[Cl:25][C:2]1[C:11]2[C:6](=[C:7]([O:12][CH3:13])[CH:8]=[CH:9][CH:10]=2)[N:5]=[C:4]([C:14]([F:17])([F:16])[F:15])[CH:3]=1

参加物

5

反応物 3

HCID 6228DimethylformamideHCID 24813Phosphorus oxychlorideHCID 178488807HCID 178488807、化合物

生成物 1

HCID 6215244-Chloro-8-methoxy-2-(trifluoromethyl)quinoline

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

4-Hydroxy-8-methoxy-2-trifluoromethylquinoline (18.77 g) is dissolved in 450 mL 8:1 CH2Cl2:DMF. POCl3 (50 mL) is added dropwise and the reaction is allowed to stir overnight. The reaction is then poured into 500 mL ice/H2O and the aqueous is extracted 2× with CH2Cl2. The organic portions are combined, washed 1× with brine, dried over MgSO4, and evaporated. The resulting oil crystallizes upon standing. The solid is recrystallized from 95% EtOH. A second crop of crystals could be obtained by concentrating down the EtOH filtrate. The total yield of product is 15.36 g.

後処理

  1. extractionthe aqueous is extracted 2× with CH2Cl2
  2. washwashed 1× with brine
  3. dry with materialdried over MgSO4
  4. customevaporated
  5. customThe resulting oil crystallizes
  6. customThe solid is recrystallized from 95% EtOH
  7. customA second crop of crystals could be obtained
  8. concentrationby concentrating down the EtOH filtrate

出典と根拠

ORDレコード
ord-0b403f17124b47b182e4888caebd1808
出典データセット
uspto-grants-2002_12
特許番号
US06500842B1

反応ノート

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