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1-[5-(4-Nitro-phenyl)-furan-2-yl]-ethanone → HCID 2302841, 화합물

HRID 1579611
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인쇄 미리보기

반응식

HRID 1579611 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]2[O:14][C:13]([C:15]([CH3:17])=[O:16])=[CH:12][CH:11]=2)=[CH:6][CH:5]=1)([O-])=O>[Ni].C(O)C>[NH2:1][C:4]1[CH:9]=[CH:8][C:7]([C:10]2[O:14][C:13]([C:15]([CH3:17])=[O:16])=[CH:12][CH:11]=2)=[CH:6][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 44054061-[5-(4-Nitro-phenyl)-furan-2-yl]-ethanone

생성물 1

HCID 2302841HCID 2302841, 화합물수율 81.5%

시약·촉매·용매 2

HCID 935Nickel촉매HCID 702Ethanol용매

실험 절차

A mixture of 58 g (0.25 mole) of methyl 5-(p-nitrophenyl)-2-furyl ketone, 2 tsp. of Raney Ni and 750 ml of ethanol was shaken under hydrogen pressure for one hour with the theoretical amount of H2 being absorbed. An additional 2000 ml of ethanol was added to the reaction mixture. The mixture was heated to reflux and the catalyst was removed by filtration. The filtrate was treated with ethereal HCl and the resulting solid was filtered and air-dried to yield 41 g (8.15%) of methyl 5-(p-aminophenyl)-2-furyl ketone. An analytical sample was prepared by drying a sample at room temperature in the vacuum pistol, m.p. scinters above 160°.

후처리

  1. customabsorbed
  2. additionAn additional 2000 ml of ethanol was added to the reaction mixture
  3. temperatureThe mixture was heated
  4. temperatureto reflux
  5. customthe catalyst was removed by filtration
  6. additionThe filtrate was treated with ethereal HCl
  7. filtrationthe resulting solid was filtered
  8. customair-dried

출처 및 근거

ORD 기록
ord-b1f74e838cd24402931dc1631eb560d6
출처 데이터셋
uspto-grants-1976_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03931247

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