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Potassium Hydroxide → HCID 19370337、化合物

HRID 129758
ノート
印刷プレビュー

反応式

HRID 129758 の反応式
[C:1]1([CH:7]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[N:8]2[CH2:13][CH2:12][N:11]([CH2:14][CH2:15][N:16](C(OCC)=O)[CH3:17])[CH2:10][CH2:9]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH-].[K+]>C(O)CO>[C:23]1([CH:7]([C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)[N:8]2[CH2:9][CH2:10][N:11]([CH2:14][CH2:15][NH:16][CH3:17])[CH2:12][CH2:13]2)[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=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

4

反応物 2

HCID 14797Potassium HydroxideHCID 19370347HCID 19370347、化合物

生成物 1

HCID 19370337HCID 19370337、化合物収率 88%

試薬・触媒・溶媒 1

HCID 174Ethylene Glycol溶媒

反応条件

温度
140 °C

実験手順

A solution of 1.6 g of 4-diphenylmethyl-1-[2-(N-ethoxycarbonyl-N-methylamino)ethyl]piperazine (prepared as described in Preparation 35') in 20 ml of a 10% w/v aqueous solution of potassium hydroxide and 20 ml of ethylene glycol was stirred at 140° C. for 20 hours. At the end of this time, the mixture was cooled to room temperature, poured into ice-water and extracted with methylene chloride. The extracts were combined, washed with water and dried over anhydrous sodium sulfate. Evaporation of the solvent under reduced pressure gave 1.14 g (yield 88%) of the title compound as an oil.

後処理

  1. temperatureAt the end of this time, the mixture was cooled to room temperature
  2. extractionextracted with methylene chloride
  3. washwashed with water
  4. dry with materialdried over anhydrous sodium sulfate
  5. customEvaporation of the solvent under reduced pressure

出典と根拠

ORDレコード
ord-64c8a0782e024cbb830c96c12d556c53
出典データセット
uspto-grants-1995_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05470851

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