反応式
[CH3:1][C:2]1([C:12]([O:14][CH2:15][CH3:16])=[O:13])[CH2:11][CH2:10][C:5]2(OCC[O:6]2)[CH2:4][CH2:3]1.CCO.O.Cl>O1CCOCC1>[CH3:1][C:2]1([C:12]([O:14][CH2:15][CH3:16])=[O:13])[CH2:3][CH2:4][C:5](=[O:6])[CH2:10][CH2:11]1参加物
6
実験手順
In a 50 mL round-bottom flask was mixed with ethyl 8-methyl-1,4-dioxaspiro[4.5]decane-8-carboxylate (Int-6a, 1.99 g, 8.72 mmol), EtOH (10 mL), H2O (5 mL), and 4N HCl in 1,4-dioxane (5 mL). The resulting solution was stirred at room temperature for 64 hours. At this time, the solvent was removed in vacuo and the residue was taken up in DCM. The suspension was washed with saturated NaHCO3(aq) and the organic layer was dried over Na2SO4. The resulting product was taken on without further purification. Yield=1.00 g.
後処理
- customAt this time, the solvent was removed in vacuo
- washThe suspension was washed with saturated NaHCO3(aq)
- dry with materialthe organic layer was dried over Na2SO4
- customThe resulting product was taken on without further purification
出典と根拠
- ORDレコード
- ord-d027fab779754691829fdfd85cf0c6a8
- 出典データセット
- uspto-grants-2013_12
- 特許番号
- US08609675B2
関連ノート
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