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Phosphorus oxychloride → 1-Chloro-6-ethoxyisoquinoline

HRID 1511466
ノート
印刷プレビュー

反応式

HRID 1511466 の反応式
[CH2:1]([O:3][C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][CH:13]=1)[C:10](=O)[NH:9][CH:8]=[CH:7]2)[CH3:2].P(Cl)(Cl)([Cl:17])=O>>[Cl:17][C:10]1[C:11]2[C:6](=[CH:5][C:4]([O:3][CH2:1][CH3:2])=[CH:13][CH:12]=2)[CH:7]=[CH:8][N:9]=1
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 24813Phosphorus oxychlorideHCID 578930896-Ethoxyisoquinolin-1(2H)-one

生成物 1

HCID 578931101-Chloro-6-ethoxyisoquinoline収率 88%

反応条件

温度
110 °C

実験手順

A suspension of 6-ethoxy-2H-isoquinolin-1-one (896 mg, 4.74 mmol) in phosphorus oxychloride (POCl3, 4 mL) was heated at 110° C. for 3 hours (clear solution obtained upon heating). After 3 hours, the reaction mixture was concentrated under reduced pressure. The residue was poured into iced water (10 mL), the pH adjusted to 10 with 3N sodium hydroxide, and the mixture extracted with chloroform (3×25 mL). The combined chloroform layers were washed with brine and dried over magnesium sulfate. The organic layer was then filtered and concentrated under reduced pressure to give 1-chloro-6-ethoxy-isoquinoline (866 mg, 4.18 mmol, 88% yield, >90% pure) as tan solid. MS m/z 208 (M++H).

後処理

  1. custom(clear solution obtained upon heating)
  2. concentrationthe reaction mixture was concentrated under reduced pressure
  3. additionThe residue was poured into iced water (10 mL)
  4. extractionthe mixture extracted with chloroform (3×25 mL)
  5. washThe combined chloroform layers were washed with brine
  6. dry with materialdried over magnesium sulfate
  7. filtrationThe organic layer was then filtered
  8. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-37e211e471ad46f1ac661e27fb972608
出典データセット
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08211897B2

反応ノート

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