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

2-Phenylhydrazinecarboxaldehyde → 1-methyl-2-phenylhydrazine

HRID 1952766
ノート
印刷プレビュー

反応式

HRID 1952766 の反応式
[C:1]1([NH:7][NH:8][CH:9]=O)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>O1CCCC1.CCOCC>[CH3:9][NH:8][NH:7][C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 121542-PhenylhydrazinecarboxaldehydeHCID 21226445Aluminium lithium hydride

生成物 1

HCID 101978131-methyl-2-phenylhydrazine収率 76.3%

試薬・触媒・溶媒 2

HCID 3283Diethyl Ether溶媒HCID 8028Tetrahydrofuran溶媒2 回

実験手順

A solution of N'-phenylformohydrazide (20.59 g) in dry tetrahydrofuran (750 ml) was added dropwise under nitrogen to a stirred suspension of lithium aluminium hydride (10 g) in dry tetrahydrofuran (200 ml), then the mixture was stirred and heated under reflux for 4 hours. The mixture was quenched by the slow dropwise addition of water (10 ml), followed by 5M aqueous sodium hydroxide solution (10 ml), then water (20 ml), then it was filtered, dried (MgSO4) and the solvent removed in vacuo to yield an oil. The oil was dissolved in ether, redried (MgSO4) and the solvent removed in vacuo to yield 1-methyl-2-phenylhydrazine (14.1 g) as a yellow oil.

後処理

  1. temperatureheated
  2. temperatureunder reflux for 4 hours
  3. customThe mixture was quenched by the slow dropwise addition of water (10 ml)
  4. filtrationwater (20 ml), then it was filtered
  5. dry with materialdried (MgSO4)
  6. customthe solvent removed in vacuo
  7. customto yield an oil
  8. dry with materialredried (MgSO4)
  9. customthe solvent removed in vacuo

出典と根拠

ORDレコード
ord-b7104568c8a149abbeed6e3faddea091
出典データセット
uspto-grants-2000_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06114334

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