ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Iodine → 5-Iodo-2-(methoxymethyl)-4-methyl-1H-imidazole

HRID 1488101
ノート
印刷プレビュー

反応式

HRID 1488101 の反応式
[CH3:1][O:2][CH2:3][C:4]1[NH:5][CH:6]=[C:7]([CH3:9])[N:8]=1.[I:10]I>[OH-].[Na+].ClCCl>[I:10][C:6]1[NH:5][C:4]([CH2:3][O:2][CH3:1])=[N:8][C:7]=1[CH3:9]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 807IodineHCID 178494676HCID 178494676、化合物2 回

生成物 1

HCID 1784946745-Iodo-2-(methoxymethyl)-4-methyl-1H-imidazole収率 32%

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒HCID 14798Sodium Hydroxide溶媒

実験手順

Into a 100-mL round-bottom flask, was placed a solution of 2-(methoxymethyl)-4-methyl-1H-imidazole (compound 222.2, 1.9 g, 15.06 mmol) in sodium hydroxide aqueous solution (30 mL, 2M). This was followed by the addition of a solution of iodine (7.7 g, 30.34 mmol) in dichloromethane (30 mL). The reaction mixture was stirred for 1 h at room temperature. The aqueous phase was collected and the pH was adjusted to 4 with hydrogen chloride (2M). The reaction mixture was extracted with 4×30 mL of dichloromethane and the organic layers combined. The resulting mixture was washed with 2×20 mL of sodium sulfite (sat.) and 3×30 mL of brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. This resulted in 1.2 g (32%) of the title compound as a yellow solid.

後処理

  1. customInto a 100-mL round-bottom flask, was placed
  2. customThe aqueous phase was collected
  3. extractionThe reaction mixture was extracted with 4×30 mL of dichloromethane
  4. washThe resulting mixture was washed with 2×20 mL of sodium sulfite (sat.) and 3×30 mL of brine
  5. dry with materialdried over anhydrous sodium sulfate
  6. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-068943e911734acbac9f19ddd17c08bf
出典データセット
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09428502B2

反応ノート

読み込み中…

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