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Potassium Carbonate → ethyl-5-[(2-oxocyclohexyl)oxy]-1H-pyrazole-3-carboxylate

HRID 1744988
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HRID 1744988 반응식
[OH:1][C:2]1[NH:6][N:5]=[C:4]([C:7]([O:9][CH2:10][CH3:11])=[O:8])[CH:3]=1.C(=O)([O-])[O-].[K+].[K+].Cl[CH:19]1[CH2:24][CH2:23][CH2:22][CH2:21][C:20]1=[O:25]>C(#N)C>[CH2:10]([O:9][C:7]([C:4]1[CH:3]=[C:2]([O:1][CH:19]2[CH2:24][CH2:23][CH2:22][CH2:21][C:20]2=[O:25])[NH:6][N:5]=1)=[O:8])[CH3:11]
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참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 132032-ChlorocyclohexanoneHCID 178469373HCID 178469373, 화합물

생성물 1

HCID 178469286ethyl-5-[(2-oxocyclohexyl)oxy]-1H-pyrazole-3-carboxylate수율 49%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

To the stirred suspension of ethyl 5-hydroxy-1H-pyrazole-3-carboxylate (6.25 g, 40 mmol) and 22.1 g of potassium carbonate in 500 ml of acetonitrile was added 6.35 g of 2-chlorocyclohexanone, and refluxed for 16 hours. The reaction mixture was allowed to cool to room temperature, then filtered, the solid was washed with acetonitrile. The filtrate was concentrated to an oil. The residue was dissolved in ethyl acetate and extracted with water. The organic phase was dried over MgSO4 and evaporated to dryness. The product was purified by silics-gel column chromatography by eluting it with 1:1 ethyl acetaet;hexane. 4.92 g (49%) of the desired product was obtained as a white solid. M.Pt. 122–124° C.; (M+H) 253.

후처리

  1. temperaturerefluxed for 16 hours
  2. filtrationfiltered
  3. washthe solid was washed with acetonitrile
  4. concentrationThe filtrate was concentrated to an oil
  5. dissolutionThe residue was dissolved in ethyl acetate
  6. extractionextracted with water
  7. dry with materialThe organic phase was dried over MgSO4
  8. customevaporated to dryness
  9. customThe product was purified by silics-gel column chromatography
  10. washby eluting it with 1:1 ethyl acetaet

출처 및 근거

ORD 기록
ord-195d00cdb62041838635a508859b8b29
출처 데이터셋
uspto-grants-2006_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07018997B2

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