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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Ethanol → HCID 86738169, 화합물

HRID 1660299
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HRID 1660299 반응식
[C:1]([NH2:5])(=[O:4])[CH:2]=[CH2:3].[CH2:6]([N:9](CC=C)[CH:10]=[CH:11][CH:12]=[C:13]([C:16]#[N:17])[C:14]#[N:15])[CH:7]=[CH2:8].C(O)C>O>[C:1]([NH2:5])(=[O:4])[CH:2]=[CH2:3].[CH2:6]([NH:9][CH:10]=[CH:11][CH:12]=[C:13]([C:14]#[N:15])[C:16]#[N:17])[CH:7]=[CH2:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 702Ethanol5회HCID 6579Acrylamide5회HCID 53724731{3-[Di(prop-2-en-1-yl)amino]prop-2-en-1-ylidene}propanedinitrile

생성물 1

HCID 86738169HCID 86738169, 화합물

시약·촉매·용매 1

HCID 962Water용매2회

실험 절차

A solution of 120 g. of acrylamide and 114 g. of 3-diallylaminoallylidenemalononitrile (A) in 500 cc. of ethanol was refluxed. 3.2 g. of AZBN were added and the solution was refluxed for one hour under stirring. A solution of 104 g. of acrylamide, 800 cc. of ethanol and 3.2 g. of AZBN was added and the solution was refluxed for one hour under stirring. A solution of 88 g. of acrylamide, 400 cc. of ethanol and 2.4 g. of AZBN was added and refluxed for one hour. A solution of 72 g. of acrylamide, 400 cc. of ethanol and 1.6 g. of AZBN was added and the solution was refluxed for one hour. In conclusion a solution of 56 g. of acrylamide, 400 cc. of ethanol and 1.6 g. of AZBN was added and refluxed for 2 hours. The mixture was cooled, filtered, washed with ethanol and then with ethyl ether and vacuum dried at 50° C. 478 g. of a product containing about 9% aminoallylidenemalononitrile units in weight were obtained, the product solution at 6% in water diluted 1:2000 with water had an optical density of 0.76 at 382 nm.

후처리

  1. additionof AZBN were added
  2. temperaturethe solution was refluxed for one hour
  3. additionof AZBN was added
  4. temperaturethe solution was refluxed for one hour
  5. stirringunder stirring
  6. additionof AZBN was added
  7. temperaturerefluxed for one hour
  8. additionof AZBN was added
  9. temperaturethe solution was refluxed for one hour
  10. additionof AZBN was added
  11. temperaturerefluxed for 2 hours
  12. temperatureThe mixture was cooled
  13. filtrationfiltered
  14. washwashed with ethanol
  15. dry with materialwith ethyl ether and vacuum dried at 50° C
  16. additionof a product containing about 9% aminoallylidenemalononitrile units in weight
  17. customwere obtained

출처 및 근거

ORD 기록
ord-3fee23e315c044148688b8969c9d5fa9
출처 데이터셋
uspto-grants-1981_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04307184

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