反応式
C(O[C:4]([C:6](C)([C:15](=[O:17])[CH3:16])[CH2:7][CH2:8][CH2:9][CH2:10][S:11]([O-:14])(=[O:13])=[O:12])=O)C.[Na]>Cl>[CH3:4][CH:6]([C:15](=[O:17])[CH3:16])[CH2:7][CH2:8][CH2:9][CH2:10][S:11]([OH:14])(=[O:12])=[O:13]参加物
4
実験手順
5-(Ethoxycarbonyl)-5-methyl-6-oxoheptane-1-sulphonate, sodium salt (from 1.1) was heated at 90° C. in concentrated hydrochloric acid (200 ml), until TLC indicated complete reaction (˜3 hrs). The solvent was then evaporated under vacuum; the residue was purified by flash chromatography (Silica. Ethanol/dichloromethane mixtures) to give 49.6 g of 5-methyl-6-oxoheptane-1-sulphonic acid.
後処理
- customreaction (˜3 hrs)
- customThe solvent was then evaporated under vacuum
- customthe residue was purified by flash chromatography (Silica. Ethanol/dichloromethane mixtures)
出典と根拠
- ORDレコード
- ord-d343bf7b98de416fb47c01395140dd59
- 出典データセット
- uspto-grants-2010_08
- 特許番号
- US07767829B2
関連ノート
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