ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Phosphorus oxychloride → 1-Chloro-6-ethoxyisoquinoline

HRID 1895866
ノート
印刷プレビュー

反応式

HRID 1895866 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].O=P(Cl)(Cl)[Cl:17]>>[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 POCl3 (4 mL) was heated at 110° C. for 3 h (clear solution obtained upon heating). After 3 h, the reaction mixture was concentrated under reduced pressure. The residue was poured into iced water (10 mL), pH was then adjusted to 10 with 3N NaOH and extracted with CHCl3 (3×25 mL). The combined CHCl3 layers were washed with brine and dried (MgSO4). The organic layer was then filtered and concentrated 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

  • custom(clear solution obtained upon heating)
  • concentrationthe reaction mixture was concentrated under reduced pressure
  • additionThe residue was poured into iced water (10 mL), pH
  • extractionextracted with CHCl3 (3×25 mL)
  • washThe combined CHCl3 layers were washed with brine
  • dry with materialdried (MgSO4)
  • filtrationThe organic layer was then filtered
  • concentrationconcentrated
  • 出典と根拠

    ORDレコード
    ord-4e2afd8362864769bffc312bc51ba35f
    出典データセット
    uspto-grants-2013_08
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US08518874B2

    反応ノート

    読み込み中…

    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