Hydrochloric Acid → Ethyl 2,2-dimethylbutanoate
反応式
Cl.[CH3:2][C:3]([CH3:9])([CH2:7][CH3:8])[C:4]([OH:6])=[O:5].O.[CH2:11](O)[CH3:12]>>[CH2:11]([O:5][C:4](=[O:6])[C:3]([CH3:9])([CH3:2])[CH2:7][CH3:8])[CH3:12]参加物
5
実験手順
Add 0.2 mL of concentrated hydrochloric acid to 2,2-dimethyl-butanoic acid (5.0 g, 43.0 mmol) in ethanol (43 mL) and heat to reflux for 5 hours. Cool to room temperature. Pour the reaction into water and extract with diethyl ether. Wash the combined organics with saturated aqueous sodium bicarbonate and water, dry over magnesium sulfate, filter, and concentrate under reduced pressure to afford the title compound which was used without further purification (4.0 g, 64.4%): 1H NMR (CDCl3) δ 0.82 (t, 3H, 1.14 (s, 3H), 1.23 (t, 3H), 1.55 (q, 2H), 4.1 (q, 2H).
後処理
- temperatureheat
- temperatureto reflux for 5 hours
- additionPour
- extractionextract with diethyl ether
- washWash the combined organics with saturated aqueous sodium bicarbonate and water
- dry with materialdry over magnesium sulfate
- filtrationfilter
- concentrationconcentrate under reduced pressure
出典と根拠
- ORDレコード
- ord-59e87af6c13d4a4197ab5e5aa2efb6b9
- 出典データセット
- uspto-grants-2013_11
- 特許番号
- US08592590B2
反応ノート
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