Acetone → Diallyl sulfone
反応式
[CH2:1](O)[CH:2]=[CH2:3].O[O:6][S:7]([O-:9])=O.[K+].[CH3:11][C:12]([CH3:14])=O>O>[CH2:1]([S:7]([CH2:14][CH:12]=[CH2:11])(=[O:9])=[O:6])[CH:2]=[CH2:3]参加物
5
実験手順
A solution of allyl alcohol isomer A from Step 2 (7.11 g, 16.65 mmol) and oxone (30.75 g, 50.0 mmol) in acetone (100 mL) and water (25 mL) was stirred at RT overnight then filtered, diluted with water and AcOEt, extracted with AcOEt, dried and concentrated. The residue is purified was purified by flash-chromatography over silica gel (eluted with Hexanes/AcOEt 99:1 to 60:40) to provide 5.50 g (72%) of allylsulfone.
後処理
- filtrationthen filtered
- additiondiluted with water and AcOEt
- extractionextracted with AcOEt
- customdried
- concentrationconcentrated
- customThe residue is purified
- customwas purified by flash-chromatography over silica gel (eluted with Hexanes/AcOEt 99:1 to 60:40)
出典と根拠
- ORDレコード
- ord-d6e63dc26e2248b4b93a5bb95fa6cb07
- 出典データセット
- uspto-grants-2011_11
- 特許番号
- US08067621B2
反応ノート
読み込み中…