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O-Toluidine → HCID 10357805, 화합물

HRID 1647489
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HRID 1647489 반응식
[C:1]([C:5]1[CH:6]=[N:7][C:8]2[C:13]([C:14]=1Cl)=[CH:12][CH:11]=[CH:10][C:9]=2[OH:16])(=[O:4])[CH2:2][CH3:3].[CH3:17][C:18]1[CH:24]=[CH:23][CH:22]=[CH:21][C:19]=1[NH2:20]>O1CCOCC1>[C:1]([C:5]1[CH:6]=[N:7][C:8]2[C:13]([C:14]=1[NH:20][C:19]1[CH:21]=[CH:22][CH:23]=[CH:24][C:18]=1[CH3:17])=[CH:12][CH:11]=[CH:10][C:9]=2[OH:16])(=[O:4])[CH2:2][CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7242O-ToluidineHCID 10263493HCID 10263493, 화합물

생성물 1

HCID 10357805HCID 10357805, 화합물

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

Impure 3-propanoyl-4-chloro-8-hydroxyquinoline (86 g) and 2-methylaniline (10.7 ml) in dioxan (200 ml) were warmed over a steam bath for 30 minutes, then left to stand overnight. After evaporation of the dioxan, dichloromethane and aqueous sodium bicarbonate were added, the organic layer washed with water and brine, dried and evaporated to a yellow solid. Recrystallisation from methanol gave 3-propanoyl-4-(2-methylphenylamino)-8-hydroxyquinoline (11.6 g), m.p. 125°-128°.

후처리

wait
left
  • customAfter evaporation of the dioxan, dichloromethane and aqueous sodium bicarbonate
  • additionwere added
  • washthe organic layer washed with water and brine
  • customdried
  • customevaporated to a yellow solid
  • customRecrystallisation from methanol
  • 출처 및 근거

    ORD 기록
    ord-8b14e82cbb594fed869b9a9a4b0137c4
    출처 데이터셋
    uspto-grants-1995_07
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05432182

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