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Methyl iodide → HCID 86721227, 화합물

HRID 1750386
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HRID 1750386 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:12]([C:13]([O:15][CH2:16][CH3:17])=[O:14])=[CH:11][NH:10][N:9]=2)=[CH:4][CH:3]=1.[H-].[Na+].[CH3:20]I>C1COCC1>[F:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[N:9]([CH3:20])[N:10]=[CH:11][C:12]=2[C:13]([O:15][CH2:16][CH3:17])=[O:14])=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 178469915HCID 178469915, 화합물

생성물 1

HCID 86721227HCID 86721227, 화합물수율 90%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of ethyl 3-(4-fluorophenyl)-1H-pyrazole-4-carboxylate (15.0 g, 64.0 mmol) in THF was added sodium hydride (55 wt % paraffin oil, 3.35 g, 77.0 mmol) at room temperature and methyl iodide (8.01 mL, 128 mmol) was successively added at room temperature. After stirring at room temperature for 15 min, the reaction mixture was poured into ice water. The mixture was extracted with ethyl acetate, the organic layer was washed with saturated brine and dried, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (solvent; 33% ethyl acetate/hexane) to give a mixture (1:1 (mol/mol), 14.2 g, 90%) of ethyl 5-(4-fluorophenyl)-1-methyl-1H-pyrazole-4-carboxylate and ethyl 3-(4-fluorophenyl)-1-methyl-1H-pyrazole-4-carboxylate as a brown oil.

후처리

  1. extractionThe mixture was extracted with ethyl acetate
  2. washthe organic layer was washed with saturated brine
  3. customdried
  4. customthe solvent was evaporated under reduced pressure
  5. customThe residue was purified by silica gel column chromatography (solvent; 33% ethyl acetate/hexane)

출처 및 근거

ORD 기록
ord-c1553e038b6a4bfb9932cc40ca47fd27
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09156837B2

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