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Chloroacetyl chloride → HCID 11107745、化合物

HRID 232704
ノート
印刷プレビュー

反応式

HRID 232704 の反応式
[Cl:1][CH2:2][C:3](Cl)=[O:4].[Cl-].[Al+3].[Cl-].[Cl-].[CH2:10]([C:12]1[CH:13]=[CH:14][CH:15]=[C:16]2[C:21]=1[NH:20][C:19](=[O:22])[CH:18]=[CH:17]2)[CH3:11]>C(=S)=S>[Cl:1][CH2:2][C:3]([C:14]1[CH:15]=[C:16]2[C:21](=[C:12]([CH2:10][CH3:11])[CH:13]=1)[NH:20][C:19](=[O:22])[CH:18]=[CH:17]2)=[O:4]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 6577Chloroacetyl chlorideHCID 6451240Aluminum(III) ChlorideHCID 108668132(1H)-Quinolinone, 8-ethyl-

生成物 1

HCID 11107745HCID 11107745、化合物

試薬・触媒・溶媒 1

HCID 6348Carbon Disulfide溶媒

実験手順

To a solution of 62 ml of chloroacetyl chloride in 600 ml of carbon disulfide were added, with ice-cooling, 173 g of aluminum chloride and 44 g of 8-ethylcarbostyril in this order. The mixture was refluxed for 6 hours. The reaction mixture was subjected to distillation to remove carbon disulfide. The residue was poured into ice water. The mixture was stirred at room temperature overnight. The insoluble portion was collected by filtration, washed with water and dried to obtain 55 g of 6-chloroacetyl-8-ethylcarbostyril as a brown powder.

後処理

  1. temperaturecooling
  2. temperatureThe mixture was refluxed for 6 hours
  3. distillationThe reaction mixture was subjected to distillation
  4. customto remove carbon disulfide
  5. additionThe residue was poured into ice water
  6. filtrationThe insoluble portion was collected by filtration
  7. washwashed with water
  8. customdried

出典と根拠

ORDレコード
ord-379c6a31a2e94220a350956cae039110
出典データセット
uspto-grants-1997_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05591751

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート