Acetic Acid → methyl 3-cyclopropyl-2,3-epoxypropionate
反応式
C[O-].[Na+].[CH:4]1([CH:7]=[O:8])[CH2:6][CH2:5]1.Cl[CH2:10][C:11]([O:13][CH3:14])=[O:12].C(O)(=O)C>CO.O>[CH:4]1([CH:7]2[O:8][CH:10]2[C:11]([O:13][CH3:14])=[O:12])[CH2:6][CH2:5]1参加物
反応条件
- 温度
- -10 °C
実験手順
A 300-ml three-necked flask equipped with a thermometer and a stirrer was charged with 87 g (0.45 mole) of a 28% sodium methoxide solution in methanol and 21 g (0.30 mole) of cyclopropanecarbaldehyde and, after the contents had been cooled down to −10° C., 48.9 g (0.45 mole) of methyl chloroacetate was added dropwise over 3 hours. After completion of the addition, the reaction mixture was allowed to be warmed up to room temperature and was then stirred at room temperature for 5 hours. Thereafter, 12 g (0.20 mole) of acetic acid was added to neutralize remaining sodium methoxide and the resulting mixture was poured into 140 g of water. The reaction mixture thus obtained was extracted three times each with 50 ml of ethyl acetate and the extracts were washed with 50 ml of saturated salt water. The mixture thus washed was dried over anhydrous sodium sulfate and condensed. The residue was distilled under reduced pressure to yield, as distillates at 70 to 73° C. [6 mmHg (8.0 hPa)], 29.8 g (0.21 mole; yield: 70.0%) of methyl 3-cyclopropyl-2,3-epoxypropionate having the following properties.
後処理
- customA 300-ml three-necked flask equipped with a thermometer and a stirrer
- additionAfter completion of the addition
- temperatureto be warmed up to room temperature
- customThe reaction mixture thus obtained
- extractionwas extracted three times each with 50 ml of ethyl acetate
- washthe extracts were washed with 50 ml of saturated salt water
- washThe mixture thus washed
- dry with materialwas dried over anhydrous sodium sulfate and condensed
- distillationThe residue was distilled under reduced pressure
出典と根拠
- ORDレコード
- ord-6ffdc331deb04eb49930410b3019191e
- 出典データセット
- uspto-grants-2007_01
- 特許番号
- US07164047B2
反応ノート
読み込み中…