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Thionyl Chloride → 5-Chloromethyl-4-methyl-1-propylimidazole hydrochloride

HRID 856778
ノート
印刷プレビュー

反応式

HRID 856778 の反応式
O[CH2:2][C:3]1[N:7]([CH2:8][CH2:9][CH3:10])[CH:6]=[N:5][C:4]=1[CH3:11].S(Cl)([Cl:14])=O>>[ClH:14].[Cl:14][CH2:2][C:3]1[N:7]([CH2:8][CH2:9][CH3:10])[CH:6]=[N:5][C:4]=1[CH3:11]
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

3

反応物 2

HCID 24386Thionyl ChlorideHCID 229387645-Hydroxymethyl-4-methyl-1-propylimidazole

生成物 1

HCID 229385505-Chloromethyl-4-methyl-1-propylimidazole hydrochloride

反応条件

温度
90 °C

実験手順

To 5-hydroxymethyl-4-methyl-1-propylimidazole (2.4 g) was added thionyl chloride (10 ml) at 0° C., and the mixture was heated for 30 minutes at 90° C. The mixture was allowed to be at room temperature. The solvent was distilled off under reduced pressure and the obtained residue was dissolved in methanol. The solvent was distilled off again under reduced pressure, to give 5-chloromethyl-4-methyl-1-propylimidazole hydrochloride (3.13 g) as brown oil.

後処理

  1. customto be at room temperature
  2. distillationThe solvent was distilled off under reduced pressure
  3. dissolutionthe obtained residue was dissolved in methanol
  4. distillationThe solvent was distilled off again under reduced pressure

出典と根拠

ORDレコード
ord-3112afcb917c407aa31fbe834092ed52
出典データセット
uspto-grants-2007_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07262185B2

反応ノート

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