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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Diethyl Ether → Lytron 810

HRID 649607
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인쇄 미리보기

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HRID 649607 반응식
[C:1]1(=[O:7])[O:6][C:4](=[O:5])[CH:3]=[CH:2]1.[CH2:8]=[CH:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.C(OCC)C>C(C(C)=O)C>[CH2:8]=[CH:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.[CH:2]1[C:1](=[O:7])[O:6][C:4](=[O:5])[CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 3283Diethyl EtherHCID 7501StyreneHCID 7923Maleic Anhydride

생성물 1

HCID 62707Lytron 810수율 78.8%

시약·촉매·용매 1

HCID 6569Methyl Ethyl Ketone용매

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온도
60 °C

실험 절차

In 200 ml of methyl ethyl ketone were dissolved 19.4 g of maleic anhydride and 20.6 g of styrene, and to the solution was added 0.65 g of azobisisobutylnitrile(AIBN). The resulting mixture was heated at 60° C. for 2 hours under nitrogen atmosphere for performing polymerization. The reaction solution was then dropwise added to 500 ml of ethyl ether under stirring to precipitate a polymer. Thus precipitated polymer was collected by filtration and purified by repeating twice the THF dissolution-ethyl ether precipitation procedure described in Example 1. Thus purified polymer was dried under vacuum at 100° C. for 24 hours to give 31.5 g of a maleic anhydride-styrene copolymer. It was confiremed by elementary analysis that the copolymerization ratio was approximately 1:1. Mn was 55,400.

후처리

  1. custompolymerization
  2. customto precipitate a polymer
  3. filtrationThus precipitated polymer was collected by filtration
  4. custompurified
  5. dissolutionthe THF dissolution-ethyl ether precipitation procedure
  6. customThus purified polymer was dried under vacuum at 100° C. for 24 hours

출처 및 근거

ORD 기록
ord-cbe89f700d1d4f44be46528cfa737033
출처 데이터셋
uspto-grants-1988_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04740561

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