ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Hydrogen Peroxide → 1-{4-[1-(4-Methoxyphenyl)ethenyl]phenyl}pyrrolidine

HRID 1199114
ノート
印刷プレビュー

反応式

HRID 1199114 の反応式
[OH-].[Na+].[CH3:3][O:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]([C:16]2[CH:21]=[CH:20][C:19]([N:22]3[CH2:26][CH2:25][CH2:24][CH2:23]3)=[CH:18][CH:17]=2)(C)[C:12](O)=O)=[CH:7][CH:6]=1.OO>>[CH3:3][O:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]([C:16]2[CH:21]=[CH:20][C:19]([N:22]3[CH2:26][CH2:25][CH2:24][CH2:23]3)=[CH:18][CH:17]=2)=[CH2:12])=[CH:7][CH:6]=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 3

HCID 784Hydrogen PeroxideHCID 14798Sodium HydroxideHCID 19868034HCID 19868034、化合物

生成物 1

HCID 143237921-{4-[1-(4-Methoxyphenyl)ethenyl]phenyl}pyrrolidine収率 69.9%

実験手順

Into 50 ml of 5% aqueous solution of sodium hydroxide was dissolved 5 g of 2-(4-methoxyphenyl)-2-(4-pyrrolidinophenyl)propionic acid. Thereto was gradually added dropwise 2.4 g of 35% aqeous solution of hydrogen peroxide and the mixture was reacted at room temperature with stirring for 2 hours, and further at 60° C. with stirring for one hour. The reaction mixture was cooled and the precipitated crystal was collected by filtration. The crystal was recrystallized from methanol to give 3.0 g (yield 69.9%) of 1-(4-methoxyphenyl)-1-(4-pyrrolidinophenyl)ethylene, having a melting point of 159°~162° C.

後処理

  1. customthe mixture was reacted at room temperature
  2. stirringfurther at 60° C. with stirring for one hour
  3. temperatureThe reaction mixture was cooled
  4. filtrationthe precipitated crystal was collected by filtration
  5. customThe crystal was recrystallized from methanol

出典と根拠

ORDレコード
ord-ed73a16bc8784b1db4b579dfac80fc5e
出典データセット
uspto-grants-1990_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04898941

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート