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Sodium Hydroxide → 3-(1-Ethoxyethoxy)oxetane

HRID 1075314
ノート
印刷プレビュー

反応式

HRID 1075314 の反応式
C([O:4][CH2:5][CH:6]([O:9][CH:10]([O:12][CH2:13][CH3:14])[CH3:11])[CH2:7]Cl)(=O)C.[OH-].[Na+]>O>[CH2:13]([O:12][CH:10]([O:9][CH:6]1[CH2:5][O:4][CH2:7]1)[CH3:11])[CH3:14]
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 14798Sodium HydroxideHCID 131539053-Chloro-2-(1-ethoxyethoxy)propyl acetate

生成物 1

HCID 131539063-(1-Ethoxyethoxy)oxetane

試薬・触媒・溶媒 1

HCID 962Water溶媒2 回

反応条件

温度
25 °C

実験手順

The crude 3-chloro-2-(1-ethoxyethoxy)-1-propyl acetate produced in Example 9 was added over a period of 1.5 hours to a stirred hot (105°) solution of 1.1 kg (27.5 moles) of sodium hydroxide in 1.1 L of water in a 5 L three-necked round-bottomed flask equipped with a mechanical stirrer, a reflux condenser, a dropping funnel, and a thermometer. The mixture was refluxed for an additional 4 hours period and then was allowed to cool to 25° C. The mixture was stirred with 1.5 L of water to dissolve inorganic salts and the phases were separated. The aqueous solution was extracted with 2 L of methylene chloride. Solvent was removed from the methylene chloride layer and the residual oil was combined with the above organic phase to give 1.2 kg of crude 3-(1-ethoxyethoxy) oxetane.

後処理

  1. customequipped with a mechanical stirrer, a reflux condenser, a dropping funnel
  2. temperatureThe mixture was refluxed for an additional 4 hours period
  3. dissolutionto dissolve inorganic salts
  4. customthe phases were separated
  5. extractionThe aqueous solution was extracted with 2 L of methylene chloride
  6. customSolvent was removed from the methylene chloride layer

出典と根拠

ORDレコード
ord-c10d1dc7ddb04949acd8a22b0b4cdcac
出典データセット
uspto-grants-1983_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04395561

反応ノート

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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