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Sulfuric Acid → 7,7-Dimethyl-8-fluorodibenzo[de,h]quinoline

HRID 84136
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HRID 84136 반응식
[CH3:1][C:2]([C:5]1[C:10]([F:11])=[CH:9][CH:8]=[CH:7][C:6]=1[C:12]1[C:21]2[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=2)[CH:15]=[CH:14][N:13]=1)(O)[CH3:3].OS(O)(=O)=O.[OH-].[Na+]>ClC1C=CC=CC=1Cl>[CH3:1][C:2]1([CH3:3])[C:5]2[C:10]([F:11])=[CH:9][CH:8]=[CH:7][C:6]=2[C:12]2[N:13]=[CH:14][CH:15]=[C:16]3[CH:17]=[CH:18][CH:19]=[C:20]1[C:21]=23
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1118Sulfuric AcidHCID 14798Sodium HydroxideHCID 595226581-[2-(1-Methyl-1-hydroxyethyl)-3-fluorophenyl]isoquinoline

생성물 1

HCID 569492497,7-Dimethyl-8-fluorodibenzo[de,h]quinoline수율 75.5%

시약·촉매·용매 1

HCID 72391,2-Dichlorobenzene용매

실험 절차

26.1 g (92.82 mmol) of 1-[2-(1-methyl-1-hydroxyethyl)-3-fluorophenyl]isoquinoline were added to a mixture at 150° C. of 260 ml of o-dichlorobenzene and 104.2 ml of H2SO4, and stirred for 60 min. The reaction solution was subsequently poured onto 1000 ml of ice and adjusted cautiously to pH=12 with solid NaOH with ice cooling. Subsequently, the mixture was extracted with 500 ml of dichloromethane, dried over MgSO4 and concentrated under reduced pressure. The crude product was dissolved in 100 ml of toluene and air was introduced at 50° C. for 4 h. Subsequently, purification was effected by column chromatography with dichloromethane. 18.45 g of a solid were obtained, corresponding to 75.5% of theory, with a purity of 99.6%.

후처리

  1. extractionSubsequently, the mixture was extracted with 500 ml of dichloromethane
  2. dry with materialdried over MgSO4
  3. concentrationconcentrated under reduced pressure
  4. dissolutionThe crude product was dissolved in 100 ml of toluene
  5. additionair was introduced at 50° C. for 4 h
  6. customSubsequently, purification

출처 및 근거

ORD 기록
ord-f3c426f209f3454786741646076b5238
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08846920B2

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