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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
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Maleic Anhydride → HCID 178456689、化合物

HRID 1856452
ノート
印刷プレビュー

反応式

HRID 1856452 の反応式
[C:1]1(=[O:7])O[C:4](=[O:5])[CH:3]=[CH:2]1.S(O)(O)(=O)=O.[CH:13]([NH:16][NH2:17])([CH3:15])[CH3:14]>O.Cl>[CH:13]([N:16]1[C:4](=[O:5])[CH:3]=[CH:2][C:1]([OH:7])=[N:17]1)([CH3:15])[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

5

反応物 2

HCID 7923Maleic AnhydrideHCID 3017832Isopropylhydrazine sulphate

生成物 1

HCID 178456689HCID 178456689、化合物収率 64%

試薬・触媒・溶媒 2

HCID 313Hydrochloric Acid溶媒HCID 962Water溶媒

反応条件

温度
0 °C

実験手順

The following example illustrates the preparation of the novel compounds: ##STR6## 58.8 g (0.6 mol) of maleic anhydride were added to a solution of 73.8 g (0.6 mol) of isopropylhydrazine sulphate in 180 ml of water and 10 ml of concentrated hydrochloric acid at 60° C. The mixture was then boiled for 3 hours under reflux after which it was cooled to 0° C. After half an hour, the product which had precipitated was filtered off. 59 g (64% of theory) of 1-isopropyl-1,6-dihydro-3-hydroxy-6-oxo-pyridazine were thus obtained in the form of colorless crystals of melting point 148° C.

後処理

  1. customthe preparation of the novel compounds
  2. temperatureunder reflux after which it
  3. waitAfter half an hour
  4. customthe product which had precipitated
  5. filtrationwas filtered off

出典と根拠

ORDレコード
ord-7f33cc590a2a4d12a64df81c6faf0140
出典データセット
uspto-grants-1980_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04219546

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