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N-vinyl-2-pyrrolidone → HCID 86738171, 화합물

HRID 1660304
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HRID 1660304 반응식
[CH2:1]([N:4]([CH2:13][CH:14]=[CH2:15])[CH:5]=[CH:6][CH:7]=[C:8]([C:11]#[N:12])[C:9]#[N:10])[CH:2]=[CH2:3].[CH:16]([N:18]1[CH2:22][CH2:21][CH2:20][C:19]1=[O:23])=[CH2:17]>CN1CCCC1=O>[CH:16]([N:18]1[CH2:22][CH2:21][CH2:20][C:19]1=[O:23])=[CH2:17].[CH2:1]([N:4]([CH:5]=[CH:6][CH:7]=[C:8]([C:9]#[N:10])[C:11]#[N:12])[CH2:13][CH:14]=[CH2:15])[CH:2]=[CH2:3]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6917N-vinyl-2-pyrrolidoneHCID 53724731{3-[Di(prop-2-en-1-yl)amino]prop-2-en-1-ylidene}propanedinitrile

생성물 1

HCID 86738171HCID 86738171, 화합물

시약·촉매·용매 1

HCID 13387N-methyl-2-pyrrolidone용매

반응 조건

온도
85 °C

실험 절차

25 g of intermediate (A) and 25 g of vinylpyrrolidone were dissolved in 100 ml of N-methylpyrrolidone and added with 2.5 g of AZBN. The mixture was then heated to reflux at 85° C. for 6 hours in a flask provided with a stirrer and reflux condenser, then it was cooled, precipitated in ether and dried at 50° C. The yield was 15.7 g of a product soluble in 40:60 water-ethanol, containing about 44% w/w of aminoallylidenmalononitrile moieties.

후처리

  1. additionadded with 2.5 g of AZBN
  2. temperatureThe mixture was then heated
  3. customprovided with a stirrer
  4. temperaturereflux condenser
  5. temperatureit was cooled
  6. customprecipitated in ether
  7. customdried at 50° C
  8. additionThe yield was 15.7 g of a product soluble in 40:60 water-ethanol, containing about 44% w/w of aminoallylidenmalononitrile moieties

출처 및 근거

ORD 기록
ord-99289c3f4d5e4fb1bdee169b3377c00d
출처 데이터셋
uspto-grants-1981_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04307183

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