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Ethyl Acetate → HCID 58083493, 화합물

HRID 1254002
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HRID 1254002 반응식
[CH2:1]([N:3]1[C:7]([C:8]([O:10][CH3:11])=[O:9])=[C:6](I)[C:5]([CH3:13])=[N:4]1)[CH3:2].[Cu][C:15]#[N:16].CCOC(C)=O>CN(C=O)C>[C:15]([C:6]1[C:5]([CH3:13])=[N:4][N:3]([CH2:1][CH3:2])[C:7]=1[C:8]([O:10][CH3:11])=[O:9])#[N:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8857Ethyl AcetateHCID 58083500HCID 58083500, 화합물HCID 178418546HCID 178418546, 화합물

생성물 1

HCID 58083493HCID 58083493, 화합물수율 91.4%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a flask, methyl 1-ethyl-4-iodo-3-methylpyrazol-5-ylcarboxylate (1.00 g, 0.003 mol) was dissolved in 10 mL of DMF and copper (I) cyanide (0.46 g, 0.005 mol) was added in batches. After heating to reflux for 1 h, the mixture was separated by filtration. The filtrate was diluted with 50 mL of water, and then extracted with 50 mL of ethyl acetate. The organic layer was washed with 50 mL of saturated aqueous sodium bicarbonate solution and 50 mL of saturated brine, dried over anhydrous MgSO4 and concentrated under reduced pressure. Column chromatography (EtOAc:P.E.=1:10 as eluent) gave 0.53 g of the title compound as a yellow oil (yield 80%).

후처리

  1. temperatureAfter heating
  2. temperatureto reflux for 1 h
  3. customthe mixture was separated by filtration
  4. additionThe filtrate was diluted with 50 mL of water
  5. extractionextracted with 50 mL of ethyl acetate
  6. washThe organic layer was washed with 50 mL of saturated aqueous sodium bicarbonate solution and 50 mL of saturated brine
  7. dry with materialdried over anhydrous MgSO4
  8. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-e6a6db3d842a45a39921fc8f640ba3af
출처 데이터셋
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08455532B2

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