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Phosphorus pentachloride → 4-Chloro-7-methoxy-6-nitroquinoline-3-carbonitrile

HRID 379104
ノート
印刷プレビュー

反応式

HRID 379104 の反応式
[CH3:1][O:2][C:3]1[CH:12]=[C:11]2[C:6]([C:7](=O)[C:8]([C:13]#[N:14])=[CH:9][NH:10]2)=[CH:5][C:4]=1[N+:16]([O-:18])=[O:17].P(Cl)(Cl)(Cl)(Cl)[Cl:20]>>[Cl:20][C:7]1[C:6]2[C:11](=[CH:12][C:3]([O:2][CH3:1])=[C:4]([N+:16]([O-:18])=[O:17])[CH:5]=2)[N:10]=[CH:9][C:8]=1[C:13]#[N:14]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 24819Phosphorus pentachlorideHCID 109777094-Hydroxy-7-methoxy-6-nitroquinoline-3-carbonitrile

生成物 1

HCID 111399754-Chloro-7-methoxy-6-nitroquinoline-3-carbonitrile

反応条件

温度
165 °C

実験手順

A mixture of 5.3 g (21.6 mmol) of 1,4-dihydro-7-methoxy-6-nitro-4-oxo-quinoline-3-carbonitrile and 9 g (43.2 mmol) of phosphorous pentachloride was heated at 165° C. for 2 hours. The mixture was diluted with hexanes and the solid was collected. The solid was dissolved in 700 ml ethyl acetate and washed with cold dilute sodium hydroxide solution. The solution was dried over magnesium sulfate and filtered through a pad of silica gel giving 5.2 g of 4-chloro-7-methoxy-6-nitro-quinoline-3-carbonitrile as a tan solid.

後処理

  1. customthe solid was collected
  2. dissolutionThe solid was dissolved in 700 ml ethyl acetate
  3. washwashed with cold dilute sodium hydroxide solution
  4. dry with materialThe solution was dried over magnesium sulfate
  5. filtrationfiltered through a pad of silica gel giving 5.2 g of 4-chloro-7-methoxy-6-nitro-quinoline-3-carbonitrile as a tan solid

出典と根拠

ORDレコード
ord-953e2560e9b14a61aadc14f9155b5fb0
出典データセット
uspto-grants-2001_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06297258B1

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート