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Water → HCID 15239439, 화합물

HRID 1609494
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HRID 1609494 반응식
C[O:2][C:3]1[CH:8]=[CH:7][C:6]([CH:9]2[CH2:18][C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[C:11](=[O:19])[N:10]2[CH3:20])=[CH:5][CH:4]=1.[Cl-].[Al+3].[Cl-].[Cl-].O>C1C=CC=CC=1>[OH:2][C:3]1[CH:4]=[CH:5][C:6]([CH:9]2[CH2:18][C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[C:11](=[O:19])[N:10]2[CH3:20])=[CH:7][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 6451240Aluminum(III) ChlorideHCID 134476023-(4-Methoxyphenyl)-2-methyl-3,4-dihydroisoquinolin-1(2H)-one

생성물 1

HCID 15239439HCID 15239439, 화합물수율 56.4%

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

To 500 ml of a solution containing 10 g of 3-(4-methoxyphenyl)-2-methyl-1-oxo-1,2,3,4-tetrahydroisoquinoline in benzene, 20 g of aluminum chloride was added and the mixture was heated to reflux for 7 hours. After allowing the resulting mixture to cool, water was added thereto and the generated insoluble materials were removed by filtration through Celite. The filtrate was extracted with ethyl acetate and the combined organic layers were washed with brine, followed by drying over anhydrous magnesium sulfate. After evaporating the solvent, the residue was purified by silica gel column chromatography [hexane/ethyl acetate (2/1) to obtain 5.34 g of 3-(4-hydroxyphenyl)-2-methyl-1-oxo-1,2,3,4-tetrahydroisoquinoline.

후처리

  1. additionwas added
  2. temperaturethe mixture was heated
  3. temperatureto reflux for 7 hours
  4. temperatureto cool
  5. customthe generated insoluble materials were removed by filtration through Celite
  6. extractionThe filtrate was extracted with ethyl acetate
  7. washthe combined organic layers were washed with brine
  8. dry with materialby drying over anhydrous magnesium sulfate
  9. customAfter evaporating the solvent
  10. customthe residue was purified by silica gel column chromatography [hexane/ethyl acetate (2/1)

출처 및 근거

ORD 기록
ord-60017ae55f474b1bbf50e1ab4d989e70
출처 데이터셋
uspto-grants-1995_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05401752

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