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Diphenyl Ether → 4(1H)-Quinolinone, 8-methoxy-3-(1-oxobutyl)-

HRID 1382258
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HRID 1382258 반응식
[C:1]([C:6](=[CH:12][NH:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=1[O:20][CH3:21])[C:7]([O:9]CC)=O)(=[O:5])[CH2:2][CH2:3][CH3:4].C1(OC2C=CC=CC=2)C=CC=CC=1>CCOCC>[C:1]([C:6]1[C:7](=[O:9])[C:19]2[C:14](=[C:15]([O:20][CH3:21])[CH:16]=[CH:17][CH:18]=2)[NH:13][CH:12]=1)(=[O:5])[CH2:2][CH2:3][CH3:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7583Diphenyl EtherHCID 178450493HCID 178450493, 화합물

생성물 1

HCID 103321024(1H)-Quinolinone, 8-methoxy-3-(1-oxobutyl)-

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

Ethyl 2-butyryl-3-(2-methoxyphenylamino)acrylate (15.50 g, 0.053 mol) was added in portions to boiling diphenyl ether (400 ml) and the mixture heated under reflux for 1.5 hours. After cooling, the solution was diluted with ether and petroleum ether, filtered, and the solid washed with petroleum ether to give 3-butyryl-8-methoxy-4-(1H)-quinolone as light grey crystals (13.46 g, 63.1%). m.p. 200°-202°.

후처리

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temperature
the mixture heated
  • temperatureunder reflux for 1.5 hours
  • temperatureAfter cooling
  • filtrationfiltered
  • washthe solid washed with petroleum ether
  • 출처 및 근거

    ORD 기록
    ord-b1f788db9007461983454ec9c9986ea8
    출처 데이터셋
    uspto-grants-1989_02
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04806549

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