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

Iodoethane → HCID 21191829、化合物

HRID 1069463
ノート
印刷プレビュー

反応式

HRID 1069463 の反応式
[H-].[Na+].[CH3:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[NH:10][C:11](=[O:14])[O:12][CH3:13].[CH2:15](I)[CH3:16]>CN(C)C=O>[CH2:15]([N:10]([C:5]1[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=1[CH3:3])[C:11](=[O:14])[O:12][CH3:13])[CH3:16]
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 3

HCID 6340IodoethaneHCID 24758Sodium hydrideHCID 519038Carbamic acid, (2-methylphenyl)-, methyl ester

生成物 1

HCID 21191829HCID 21191829、化合物

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

5.1 g (0.2 mol) of sodium hydride are added a little at a time to 30 g (0.18 mol) of methyl N-(o-methylphenyl)-carbamate (Example 1a) in 200 ml of dimethylformamide. After the evolution of gas has ceased, 30 g (0.2 mol) of ethyl iodide are added dropwise, the reaction mixture being lightly cooled in a water bath. A white solid is precipitated. After about 4 hours, the reaction mixture is diluted with water and the aqueous phase is extracted three times with ether. The organic phase is dried over MgSO4 and evaporated down. The residue is distilled. 32.5 g (0.17 mol=93%) of the title compound are obtained as a colorless oil.

後処理

  1. temperaturethe reaction mixture being lightly cooled in a water bath
  2. customA white solid is precipitated
  3. additionthe reaction mixture is diluted with water
  4. extractionthe aqueous phase is extracted three times with ether
  5. dry with materialThe organic phase is dried over MgSO4
  6. customevaporated down
  7. distillationThe residue is distilled

出典と根拠

ORDレコード
ord-9f6fc5e4ab404b69a1f43bfa95699d8a
出典データセット
uspto-grants-2001_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06252083B1

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