反応式
[C:1]1(=[O:8])[O:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.OS(O)(=O)=O.[CH3:14][OH:15]>>[CH3:14][O:15][C:6](=[O:7])[CH2:5][CH2:4][CH2:3][CH2:2][CH2:1][OH:8]参加物
4
実験手順
A solution of ε-caprolactone (11.4 g, 0.100 mol), MeOH (300 mL) and concentrated H2SO4 (5 mL) was refluxed overnight. The resulting mixture was cooled to room temperature and concentrated. Water was added to the residue and the pH was adjusted to 7 with solid NaHCO3. The aqueous layer was extracted with ether. The combined organic layers were washed with water, dried and concentrated to give 6-hydroxy-hexanoic acid methyl ester as a colorless oil, which was used in the next step without further purification.
後処理
- concentrationconcentrated
- additionWater was added to the residue
- extractionThe aqueous layer was extracted with ether
- washThe combined organic layers were washed with water
- customdried
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-aade5df588aa4d7984bc144871052427
- 出典データセット
- uspto-grants-2006_08
- 特許番号
- US07091357B2
関連ノート
読み込み中…