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

Ozone → 2,2-Dimethyl-3-(2-oxopropyl)cyclopropanecarbaldehyde

HRID 1758577
ノート
印刷プレビュー

反応式

HRID 1758577 の反応式
CN(C)C=[CH:4][CH:5]1[CH:7]([CH2:8][C:9](=[O:11])[CH3:10])[C:6]1([CH3:13])[CH3:12].[O:15]=[O+][O-]>C(Cl)Cl>[CH3:12][C:6]1([CH3:13])[CH:7]([CH2:8][C:9](=[O:11])[CH3:10])[CH:5]1[CH:4]=[O:15]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24823OzoneHCID 545240321-(3-(2-(Dimethylamino)ethenyl)-2,2-dimethylcyclopropyl)-2-propanone

生成物 1

HCID 114691882,2-Dimethyl-3-(2-oxopropyl)cyclopropanecarbaldehyde収率 84.4%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a solution 2.4 g of 1-(3-(2-(dimethylamino)ethenyl)-2,2-dimethylcyclopropyl)-2-propanone, the product of Embodiment I, in 50 ml of methylene chloride was added 0.6 g of ozone over 20 min at -80° C. The resulting mixture was purged with air and 1.5 g of triethylamine was added dropwise at -30° C. The resulting mixture, after stirring and warming to room temperature, had a negative test to starch iodide paper. The reaction mixture was poured into 25 ml 1 N hydrochloride acid solution. The resulting mixture separated into two phases and the methylene chloride phase was washed with water, dried with MgSO4, filtered and stripped to yield 1.6 g of the desired product as an oil.

後処理

  1. customThe resulting mixture was purged with air and 1.5 g of triethylamine
  2. additionwas added dropwise at -30° C
  3. additionThe reaction mixture was poured into 25 ml 1 N hydrochloride acid solution
  4. customThe resulting mixture separated into two phases
  5. washthe methylene chloride phase was washed with water
  6. dry with materialdried with MgSO4
  7. filtrationfiltered

出典と根拠

ORDレコード
ord-9f8bfae07d374a5ba4d798ad71b3b028
出典データセット
uspto-grants-1983_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04374275

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