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Water → 2-Chloro-3-methyl-1-oxo-1lambda~5~-pyridine

HRID 588370
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HRID 588370 반응식
[Cl:1][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[CH:4][N:3]=1.OO.NC(N)=[O:13].FC(F)(F)C(OC(=O)C(F)(F)F)=O.O>C(Cl)Cl>[Cl:1][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[CH:4][N+:3]=1[O-:13]
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참가 물질

6

반응물 4

HCID 962WaterHCID 9845Trifluoroacetic anhydrideHCID 31294Carbamide PeroxideHCID 876032-Chloro-3-methylpyridine

생성물 1

HCID 134316222-Chloro-3-methyl-1-oxo-1lambda~5~-pyridine수율 86%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a mixture of 2-chloro-3-methylpyridine (15 g, 118 mmol) and urea hydrogen peroxide (44.07 g, 468.5 mmol) in DCM (300 mL) was added trifluoroacetic anhydride (98.55 g, 469.2 mmol) dropwise at 0° C. The mixture was stirred at room temperature for 20 h. The mixture was then poured into water (150 mL), and the layers were separated. The organic layer was washed with saturated aqueous Na2S2O3 (20 mL), dried over Na2SO4, filtered, and the filtrate was concentrated under reduced pressure. The crude product was purified by silica gel flash chromatography (DCM:MeOH, 100:0 to 10:1) to afford the title compound (14.5 g, 86%) as a colorless solid.

후처리

  1. customthe layers were separated
  2. washThe organic layer was washed with saturated aqueous Na2S2O3 (20 mL)
  3. dry with materialdried over Na2SO4
  4. filtrationfiltered
  5. concentrationthe filtrate was concentrated under reduced pressure
  6. customThe crude product was purified by silica gel flash chromatography (DCM:MeOH, 100:0 to 10:1)

출처 및 근거

ORD 기록
ord-9b19f3851e914078a67b2c5d960f976f
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09227956B2

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