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Acetonitrile → 4-bromo-5-(4-chlorophenyl)-1-methyl-1H-imidazole

HRID 1506657
ノート
印刷プレビュー

反応式

HRID 1506657 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:9]([CH3:13])[CH:10]=CN=2)=[CH:4][CH:3]=1.C1C(=O)N([Br:21])C(=O)C1.[C:22](#[N:24])C>>[Br:21][C:22]1[N:24]=[CH:10][N:9]([CH3:13])[C:8]=1[C:5]1[CH:4]=[CH:3][C:2]([Cl:1])=[CH:7][CH:6]=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 3

HCID 6342AcetonitrileHCID 67184N-bromobutanimideHCID 10856331(4-Chlorophenyl)-1-methyl-1H-imidazole

生成物 1

HCID 251721464-bromo-5-(4-chlorophenyl)-1-methyl-1H-imidazole

反応条件

温度
0 °C

実験手順

(4-Chlorophenyl)-1-methyl-1H-imidazole (3 g, 15.5 mmol) was dissolved in ACN (150 mL) and cooled to 0° C. NBS (2.76 g, 15.5 mmol) was added in 3 portions over 5 min. The reaction was stirred at 0° C. for 20 min then let warm to ambient temperature. Solvents were removed in vacuo and the residue partitioned between EtOAc and 20% aqueous KH2PO4. The organics were separated, washed with saturated aqueous NaHCO3, and dried with saturated aqueous NaCl. Solvents were removed in vacuo and the residue purified by column chromatography on silica to provide the desired product. MS (m/z) 273.1 [M+H]+.

後処理

  1. temperaturethen let warm to ambient temperature
  2. customSolvents were removed in vacuo
  3. customthe residue partitioned between EtOAc and 20% aqueous KH2PO4
  4. customThe organics were separated
  5. washwashed with saturated aqueous NaHCO3
  6. dry with materialdried with saturated aqueous NaCl
  7. customSolvents were removed in vacuo
  8. customthe residue purified by column chromatography on silica

出典と根拠

ORDレコード
ord-41c6eccd80504082ae7e6b03564163d4
出典データセット
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09220710B2

反応ノート

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