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

Hydrogen Peroxide → Pyridine, 3-cyclopropyl-, 1-oxide

HRID 2238668
ノート
印刷プレビュー

反応式

HRID 2238668 の反応式
[CH:1]1([C:4]2[CH:5]=[N:6][CH:7]=[CH:8][CH:9]=2)[CH2:3][CH2:2]1.[OH:10]O>C(O)(=O)C>[CH:1]1([C:4]2[CH:5]=[N+:6]([O-:10])[CH:7]=[CH:8][CH:9]=2)[CH2:3][CH2:2]1
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 784Hydrogen PeroxideHCID 120321433-cyclopropylpyridine

生成物 1

HCID 45079753Pyridine, 3-cyclopropyl-, 1-oxide収率 67.1%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

実験手順

1.93 g of 3-cyclopropylpyridine (synthesized according to a method disclosed in Tetrahedron Lett. 2002, 39, 6987-6990) was dissolved in 15 mL of acetic acid, then 2.4 g of hydrogen peroxide solution (31%) was added thereto, and heated overnight under reflux. The reaction mixture was concentrated under reduced pressure, the obtained residue was dissolved in chloroform, and washed with a saturated aqueous solution of sodium hydrogen carbonate and water in the subsequent order. The organic layer was dried over anhydrous sodium sulfate. The insolubles were filtered, the filtrate was concentrated under reduced pressure, and 1.47 g of 3-cyclopropylpyridine 1-oxide [121-1] was obtained as a brown oily product.

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

後処理

  1. temperatureheated overnight
  2. temperatureunder reflux
  3. concentrationThe reaction mixture was concentrated under reduced pressure
  4. dissolutionthe obtained residue was dissolved in chloroform
  5. washwashed with a saturated aqueous solution of sodium hydrogen carbonate and water in the subsequent order
  6. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  7. filtrationThe insolubles were filtered
  8. concentrationthe filtrate was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-86cfe41842d04ccc9becbbdf8de00f38
出典データセット
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07718801B2

反応ノート

読み込み中…