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Phosphorus oxychloride → 4-Chloro-7-(2-chlorophenyl)-5,6,7,8-tetrahydroquinolin-5-one

HRID 1700511
ノート
印刷プレビュー

反応式

HRID 1700511 の反応式
P(Cl)(Cl)([Cl:3])=O.[Cl:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[CH:13]1[CH2:22][C:21]2[NH:20][CH:19]=[CH:18][C:17](=O)[C:16]=2[C:15](=[O:24])[CH2:14]1>>[Cl:3][C:17]1[C:16]2[C:15](=[O:24])[CH2:14][CH:13]([C:8]3[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=3[Cl:6])[CH2:22][C:21]=2[N:20]=[CH:19][CH:18]=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 110656287-(2-Chlorophenyl)-1,4,5,6,7,8-hexahydroquinoline-4,5-dione

生成物 1

HCID 183177884-Chloro-7-(2-chlorophenyl)-5,6,7,8-tetrahydroquinolin-5-one収率 85.9%

反応条件

温度
100 °C

実験手順

Under ice-cooling, to phosphorus oxychloride (5.4 g) was added 7-(2-chlorophenyl)-1,4,5,6,7,8-hexahydroquinoline-4,5-dione (0.60 g), and the mixture was stirred at 100° C. for 2 hours and cooled. Under reduced pressure, phosphorus oxychloride was evaporated, and to the residue was added 1N sodium hydroxide solution. The mixture was extracted with ethyl acetate, and the organic layer was washed with water and saturated brine, dried with magnesium sulfate and concentrated under reduced pressure to give colorless crystals of 4-chloro-7-(2-chlorophenyl)-5,6,7,8-tetrahydroquinolin-5-one (0.55 g).

後処理

  1. temperaturecooled
  2. customUnder reduced pressure, phosphorus oxychloride was evaporated
  3. additionto the residue was added 1N sodium hydroxide solution
  4. extractionThe mixture was extracted with ethyl acetate
  5. washthe organic layer was washed with water and saturated brine
  6. dry with materialdried with magnesium sulfate
  7. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-f864e17c78394b11bf3094b795c01c1b
出典データセット
uspto-grants-2002_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06350749B1

反応ノート

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