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

Hydrazine hydrate (1:1) → 1H-Pyrazole, 4,5-dihydro-3-methyl-5-phenyl-

HRID 465279
ノート
印刷プレビュー

反応式

HRID 465279 の反応式
O.[NH2:2][NH2:3].[C:4]1(/[CH:10]=[CH:11]/[C:12](=O)[CH3:13])[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1>CO>[CH3:13][C:12]1[CH2:11][CH:10]([C:4]2[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=2)[NH:3][N: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

4

反応物 2

HCID 24654Hydrazine hydrate (1:1)HCID 637759Benzylideneacetone

生成物 1

HCID 101301011H-Pyrazole, 4,5-dihydro-3-methyl-5-phenyl-収率 74.8%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒2 回

実験手順

17.1 g (342 mmol) of hydrazine monohydrate was dissolved in 500 ml of methanol. Then, 50 g (342 mmol) of trans-4-phenyl-3-buten-2-one dissolved in 100 ml of methanol was gradually dropwise added thereto under stirring within a range of from 5° C. to 15° C. Then, the mixture was stirred at room temperature for 30 hours, and methanol was distilled off under reduced pressure. The residue was distilled under reduced pressure to obtain 41.0 g of the desired 3-methyl-5-phenyl-2-pyrazoline.

後処理

  1. additionwas gradually dropwise added
  2. stirringThen, the mixture was stirred at room temperature for 30 hours
  3. distillationmethanol was distilled off under reduced pressure
  4. distillationThe residue was distilled under reduced pressure

出典と根拠

ORDレコード
ord-e86188219a69483abe7df20cec0e3550
出典データセット
uspto-grants-1992_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05152824

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