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

1,4-Dioxane → HCID 12083068、化合物

HRID 1168847
ノート
印刷プレビュー

反応式

HRID 1168847 の反応式
[CH2:1]([C:5]1[C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][C:8]=2[O:7][N:6]=1)[CH2:2][CH:3]=C.[O:14]1CCOCC1.I([O-])(=O)(=O)=O.[Na+]>[Os](=O)(=O)(=O)=O.O.C(OCC)(=O)C>[O:7]1[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[C:5]([CH2:1][CH2:2][CH:3]=[O:14])=[N:6]1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 3

HCID 312751,4-DioxaneHCID 12083067HCID 12083067、化合物HCID 23667635Sodium periodate

生成物 1

HCID 12083068HCID 12083068、化合物

試薬・触媒・溶媒 3

HCID 30318Osmium Tetroxide触媒HCID 962Water溶媒2 回
HCID 8857
Ethyl Acetate
溶媒

実験手順

Compound 26 (549 mg, 3.2 mmol), water (5 mL), 1,4-dioxane (15 mL) and osmium tetroxide (15 mg, 0.06 mmol) were stirred for 5 min. in a small flask. Sodium metaperiodate (1.56 g, 7.3 mmol) was added over 30 min. and the suspension was then stirred for 1 hour. Ethyl acetate and water were added. The phases were separated and the aqueous phase was extracted with ethyl acetate and dichloromethane. The combined organic phases were dried over magnesium sulphate and evaporated to dryness to produce 784 mg of crude 27, which was used directly without further purification in the synthesis compound 28.

後処理

  1. customThe phases were separated
  2. extractionthe aqueous phase was extracted with ethyl acetate and dichloromethane
  3. dry with materialThe combined organic phases were dried over magnesium sulphate
  4. customevaporated to dryness
  5. customto produce 784 mg of crude 27, which
  6. customwas used directly without further purification in the synthesis compound 28

出典と根拠

ORDレコード
ord-16cbe03f2e3744d1a53ad3cfe2498431
出典データセット
uspto-grants-2003_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06627645B2

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