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Chlorine monoxide → 4-Chloro-8-methoxyquinoline-3-carbonitrile

HRID 612181
ノート
印刷プレビュー

反応式

HRID 612181 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][CH:6]=[C:7]2[C:12]=1[NH:11][CH:10]=[C:9]([C:13]#[N:14])[C:8]2=O.O(Cl)[Cl:17]>CN(C=O)C>[Cl:17][C:8]1[C:7]2[C:12](=[C:3]([O:2][CH3:1])[CH:4]=[CH:5][CH:6]=2)[N:11]=[CH:10][C:9]=1[C:13]#[N:14]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24646Chlorine monoxideHCID 22466766HCID 22466766、化合物

生成物 1

HCID 224666994-Chloro-8-methoxyquinoline-3-carbonitrile収率 91%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide触媒

実験手順

A mixture of 3.8 g (19 mmol) of 1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarbonitrile and 40 mL of phosphorous oxochloride and 5 drops of DMF was refluxed for 0.5 hours. The mixture was evaporated to dryness and diluted with hexanes. The solid was collected and mixed with cold dilute sodium carbonate solution and extracted several times with ethyl acetate. The organic layer was dried over sodium sulfate and filtered through a pad of silica gel. Removal of the solvent gave 3.8 g of 4-chloro-8-methoxy-3-quinolinecarbonitrile as an off white solid in 91% yield, mass spectrum (electrospray, m/e): M+H 219.1.

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

後処理

  1. temperaturewas refluxed for 0.5 hours
  2. customThe mixture was evaporated to dryness
  3. additiondiluted with hexanes
  4. customThe solid was collected
  5. additionmixed with cold dilute sodium carbonate solution
  6. extractionextracted several times with ethyl acetate
  7. dry with materialThe organic layer was dried over sodium sulfate
  8. filtrationfiltered through a pad of silica gel
  9. customRemoval of the solvent

出典と根拠

ORDレコード
ord-842fc124540245e6a9afd36f97274121
出典データセット
uspto-grants-1999_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06002008

反応ノート

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