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

Water → Ethyl [(2-methylacryloyl)amino](oxo)acetate

HRID 1073659
ノート
印刷プレビュー

反応式

HRID 1073659 の反応式
[C:1](Cl)([C:3]([O:5][CH2:6][CH3:7])=[O:4])=[O:2].[C:9]([NH2:14])(=[O:13])[C:10]([CH3:12])=[CH2:11].O>C(Cl)(Cl)Cl>[C:1]([NH:14][C:9](=[O:13])[C:10]([CH3:12])=[CH2:11])([C:3]([O:5][CH2:6][CH3:7])=[O:4])=[O:2]
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 962WaterHCID 6595MethacrylamideHCID 20884Ethoxalyl chloride

生成物 1

HCID 14298183Ethyl [(2-methylacryloyl)amino](oxo)acetate収率 28.8%

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒2 回

実験手順

Into the same reaction vessel as used in Example 1, ethoxalyl chloride (12.3 g; 0.09 mol) was charged, and the reaction vessel was cooled in an ice bath. A solution of methacrylamide (20.3 g; 0.24 mol) in chloroform (90.0 ml) was dropwise added thereto in 30 minutes, followed by stirring at room temperature for 3 days. The reaction mixture was shaken with chloroform (500 ml) and water (500 ml), and the chloroform layer was separated and dried over anhydrous magnesium sulfate, followed by removal of chloroform. Hydroquinone (0.01 g) was added thereto, and distillation under reduced pressure was carried out to give N-ethoxalylmethacrylamide (4.8 g). Yield, 29%.

後処理

  1. additionwas charged
  2. temperaturethe reaction vessel was cooled in an ice bath
  3. customthe chloroform layer was separated
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customfollowed by removal of chloroform
  6. additionHydroquinone (0.01 g) was added
  7. distillationdistillation under reduced pressure

出典と根拠

ORDレコード
ord-6ecf8ba8418942268fdcfad7e584ac07
出典データセット
uspto-grants-1990_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04970281

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