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Sodium Hydroxide → HCID 22998298、化合物

HRID 1166423
ノート
印刷プレビュー

反応式

HRID 1166423 の反応式
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[CH2:11][CH2:10][C:9]3[CH:12]=[CH:13][CH:14]=[CH:15][C:8]=3[NH:7][C:6]=2[CH:16]=1.[Cl:17][CH2:18][CH2:19][C:20](Cl)=[O:21].[OH-].[Na+]>C1(C)C=CC=CC=1>[Cl:17][CH2:18][CH2:19][C:20]([N:7]1[C:8]2[CH:15]=[CH:14][CH:13]=[CH:12][C:9]=2[CH2:10][CH2:11][C:5]2[CH:4]=[CH:3][C:2]([Cl:1])=[CH:16][C:6]1=2)=[O:21]
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

5

反応物 3

HCID 14798Sodium HydroxideHCID 693643-Chloropropionyl chloride2 回HCID 1183643-Chloroiminodibenzyl

生成物 1

HCID 22998298HCID 22998298、化合物収率 98.4%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒2 回

反応条件

温度
95 °C

実験手順

3-Chloro-10,11-dihydro-5H-dibenz[b,f]azepine (3.82 g, 16.6 mmol) was dissolved in toluene (20 ml). A solution of 3-chloropropionylchloride (2.53 g, 19.9 mmol) in toluene was added dropwise, and the resulting mixture was heated to 95° C. and stirred at that temperature for 30 minutes. The mixture was stirred overnight at room temperature. Further 3-chloropropionylchloride (2.53 g, 19.9 mmol) was added and the mixture was stirred at 95° C. for 1.5 h. After cooling, 0.2 M sodium hydroxide (10 ml) was added, and the phases were separated. The organic phase was diluted with more toluene (50 ml); and washed with first 0.2 M sodium hydroxide (6×10 ml) and then with more 0.2 M sodium hydroxide (3×20 ml) until the aqueous phase was alkaline. The organic phase was washed with water (3×15 ml), brine (25 ml), and dried (MgSO4). Evaporation in vacuo afforded 5.23 g (98%) of crude 3-chloro-1-(3-chloro-10,11-dihydro-5H-dibenz[b,f]azepin-5-yl)-1-propanone as an oil. This was further purified by addition of a mixture of heptane and ethyl acetate (1:1). This afforded 3.14 g (59%) of the product as a solid.

後処理

  1. stirringThe mixture was stirred overnight at room temperature
  2. stirringthe mixture was stirred at 95° C. for 1.5 h
  3. temperatureAfter cooling
  4. customthe phases were separated
  5. additionThe organic phase was diluted with more toluene (50 ml)
  6. washand washed with first 0.2 M sodium hydroxide (6×10 ml)
  7. washThe organic phase was washed with water (3×15 ml), brine (25 ml)
  8. dry with materialdried (MgSO4)
  9. customEvaporation in vacuo

出典と根拠

ORDレコード
ord-75b329b0379a45448be7f8c0719643e1
出典データセット
uspto-grants-2003_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06613791B1

反応ノート

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