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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Maleic Anhydride → HCID 178456689, 화합물

HRID 1856452
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HRID 1856452 반응식
[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]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 7923Maleic AnhydrideHCID 3017832Isopropylhydrazine sulphate

생성물 1

HCID 178456689HCID 178456689, 화합물수율 64%

시약·촉매·용매 2

HCID 313Hydrochloric Acid용매HCID 962Water용매

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온도
0 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-7f33cc590a2a4d12a64df81c6faf0140
출처 데이터셋
uspto-grants-1980_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04219546

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