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Dichloromethane → 4-bromo-1-(4-methoxybenzyl)-1H-imidazole

HRID 868909
ノート
印刷プレビュー

反応式

HRID 868909 の反応式
[Br:1][C:2]1[NH:6][CH:5]=[N:4][CH:3]=1.C([O-])([O-])=O.[K+].[K+].Cl[CH2:14][C:15]1[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][CH:16]=1.ClCCl>CN(C=O)C>[CH3:22][O:21][C:18]1[CH:19]=[CH:20][C:15]([CH2:14][N:4]2[CH:3]=[C:2]([Br:1])[N:6]=[CH:5]2)=[CH:16][CH:17]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 6344DichloromethaneHCID 11430Potassium CarbonateHCID 699934-Methyloxybenzyl chlorideHCID 961251H-Imidazole, 4-bromo-

生成物 1

HCID 461855504-bromo-1-(4-methoxybenzyl)-1H-imidazole収率 67.2%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒
このページの内容参加物実験手順後処理出典と根拠反応ノート

実験手順

To a suspension of 5-bromo-1H-imidazole (10 g, 68.5 mmol) and K2CO3 (37.8 g, 274 mmol) in DMF (100 mL) was added 1-(chloromethyl)-4-methoxybenzene (11.8 g, 75.4 mmol) dropwise at room temperature. The resulting mixture was stirred for 16 hours, and then dichloromethane (DCM) was added. The mixture was successively washed with water and brine, dried and concentrated to give a residue that was purified by column chromatography to afford 12.3 g of the desired compound as a solid. LC-MS: m/z 267 (M+H+).

後処理

  1. washThe mixture was successively washed with water and brine
  2. customdried
  3. concentrationconcentrated
  4. customto give a residue that
  5. customwas purified by column chromatography

出典と根拠

ORDレコード
ord-d07cceb076964d2a9dc13c23ab2832b1
出典データセット
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08969349B2

反応ノート

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