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

HRID 1471877
ノート
印刷プレビュー

反応式

HRID 1471877 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
0 °C

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-b105ef04ca8c49d4aeb515493f6b96dd
出典データセット
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09012478B2

反応ノート

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