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3-Methyl-5-phenyl-1H-pyrazole → 4-bromo-3-methyl-5-phenyl-1H-pyrazole

HRID 1471877
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HRID 1471877 반응식
[CH3:1][C:2]1[NH:6][N:5]=[C:4]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[CH:3]=1.[Br:13]Br>ClCCl>[Br:13][C:3]1[C:4]([C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=2)=[N:5][NH:6][C:2]=1[CH3:1]
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참가 물질

4

반응물 2

HCID 187743-Methyl-5-phenyl-1H-pyrazoleHCID 24408Bromine

생성물 1

HCID 7443354-bromo-3-methyl-5-phenyl-1H-pyrazole수율 79.2%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
0 °C

실험 절차

To a solution of 5-methyl-3-phenyl-1H-pyrazole (8.0 g, 50.6 mmol) in dichloromethane (150 mL) was added bromine (8.08 g, 50.6 mmol) dropwise at 0° C. The reaction was stirred at 0° C. for 30 min and then at room temperature for 2 h before quenching with aqueous Na2SO3 (10% w/w, 10 mL). The organic solvent was removed and the aqueous phase was extracted with EtOAc, washed with brine, dried over MgSO4, and concentrated. The residue was purified by silica gel column chromatography to give the title compound as a yellow oil (9.5 g). LCMS m/z=236.9 [M+H]+; 1H NMR (400 MHz, DMSO-d6) δ ppm 2.26 (s, 3H), 7.30-7.57 (m, 5H), 13.12 (s, 1H).

후처리

  1. customat room temperature for 2 h before quenching with aqueous Na2SO3 (10% w/w, 10 mL)
  2. customThe organic solvent was removed
  3. extractionthe aqueous phase was extracted with EtOAc
  4. washwashed with brine
  5. dry with materialdried over MgSO4
  6. concentrationconcentrated
  7. customThe residue was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-b105ef04ca8c49d4aeb515493f6b96dd
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09012478B2

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