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Phosphorus oxychloride → 1,4-Dichloro-7-(3-cyanophenyl)isoquinoline

HRID 479565
ノート
印刷プレビュー

反応式

HRID 479565 の反応式
O=P(Cl)(Cl)[Cl:3].[Cl:6][C:7]1[C:16]2[C:11](=[CH:12][C:13]([C:17]3[CH:22]=[CH:21][CH:20]=[C:19]([C:23]#[N:24])[CH:18]=3)=[CH:14][CH:15]=2)[C:10](=O)[NH:9][CH:8]=1>CC#N>[Cl:3][C:10]1[C:11]2[C:16](=[CH:15][CH:14]=[C:13]([C:17]3[CH:22]=[CH:21][CH:20]=[C:19]([C:23]#[N:24])[CH:18]=3)[CH:12]=2)[C:7]([Cl:6])=[CH:8][N:9]=1
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 24813Phosphorus oxychlorideHCID 534397463-(4-Chloro-1-oxo-1,2-dihydroisoquinolin-7-YL)benzonitrile

生成物 1

HCID 187712921,4-Dichloro-7-(3-cyanophenyl)isoquinoline収率 88.3%

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒2 回

実験手順

A solution of POCl3 (8.36 kg, 54.5 mol) in MeCN (11.5 L) was added to a suspension of 4-chloro-7-(3-cyanophenyl)isoquinolinone (7.65 kg, 27.3 mol) in boiling MeCN (65 L) under N2 over 1 hour. The mixture was heated at reflux for 11 hours and then cooled to room temperature. The mixture was slowly quenched with 1N aqueous HCl (38.3 L) and the resultant slurry stirred for 1 hour. The solid was collected by filtration, washed with MeCN (7.6 L) and dried in vacuo at 50° C. to give 1,4-dichloro-7-(3-cyanophenyl)isoquinoline (7.20 kg, 24.1 mol, 88%) as a creamy coloured solid.

後処理

  1. customover 1 hour
  2. temperatureThe mixture was heated
  3. temperatureat reflux for 11 hours
  4. customThe mixture was slowly quenched with 1N aqueous HCl (38.3 L)
  5. filtrationThe solid was collected by filtration
  6. washwashed with MeCN (7.6 L)
  7. customdried in vacuo at 50° C.

出典と根拠

ORDレコード
ord-22c7ffc8c6ba44578260f331c30d8a9c
出典データセット
uspto-grants-2003_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06645979B2

反応ノート

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