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Sodium Chloride → 5-Acetyl-8-(benzyloxy)-1,2-dihydroquinolin-2-one

HRID 14445
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HRID 14445 반응식
[C:1]([C:4]1[CH:13]=[CH:12][C:11]([OH:14])=[C:10]2[C:5]=1[CH:6]=[CH:7][C:8](=[O:15])[NH:9]2)(=[O:3])[CH3:2].C(=O)([O-])[O-].[K+].[K+].[CH2:22](Br)[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1.[Cl-].[Na+]>CN(C)C=O>[C:1]([C:4]1[CH:13]=[CH:12][C:11]([O:14][CH2:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)=[C:10]2[C:5]=1[CH:6]=[CH:7][C:8](=[O:15])[NH:9]2)(=[O:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 5234Sodium ChlorideHCID 7498Benzyl BromideHCID 11430Potassium CarbonateHCID 119838955-Acetyl-8-hydroxy-2(1H)-quinolinone

생성물 1

HCID 133754445-Acetyl-8-(benzyloxy)-1,2-dihydroquinolin-2-one수율 80.6%

시약·촉매·용매 1

HCID 6228
Dimethylformamide
용매

실험 절차

To the product from step (b) (37.7 g, 186 mmol) was added N,N-dimethylformamide (200 mL) and potassium carbonate (34.5 g, 250 mmol) followed by benzyl bromide (31.8 g, 186 mmol). The mixture was stirred at room temperature for 2.25 hour and then poured into saturated sodium chloride (3.5 L) at 0° C. and stirred for 1 hour. The product was collected and dried on a Buchner funnel for 1 hour, and the resulting solids were dissolved in dichloromethane (2 L) and this mixture was dried over sodium sulfate. The solution was filtered through a pad of Celite which was then washed with dichloromethane (5×200 mL). The combined filtrate was then concentrated to dryness and the resulting solids were triturated with ether (500 mL) for 2 h. The product was collected on a Buchner funnel, washed with ether (2×250 mL) and dried under reduced pressure to give the title compound (44 g) as a powder.

후처리

  1. stirringstirred for 1 hour
  2. customThe product was collected
  3. customdried on a Buchner funnel for 1 hour
  4. dissolutionthe resulting solids were dissolved in dichloromethane (2 L)
  5. dry with materialthis mixture was dried over sodium sulfate
  6. filtrationThe solution was filtered through a pad of Celite which
  7. washwas then washed with dichloromethane (5×200 mL)
  8. concentrationThe combined filtrate was then concentrated to dryness
  9. customthe resulting solids were triturated with ether (500 mL) for 2 h
  10. customThe product was collected on a Buchner funnel
  11. washwashed with ether (2×250 mL)
  12. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-8a71909445334776964669c76eb36f61
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07732441B2

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