反応式
[Na].[C:2]1([O:9][CH3:10])[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[OH:4].[CH2:11]([O:13][C:14](=[O:22])[CH:15](Cl)[C:16]([O:18][CH2:19][CH3:20])=[O:17])[CH3:12]>C(O)C>[CH2:11]([O:13][C:14](=[O:22])[CH:15]([O:4][C:3]1[CH:5]=[CH:6][CH:7]=[CH:8][C:2]=1[O:9][CH3:10])[C:16]([O:18][CH2:19][CH3:20])=[O:17])[CH3:12]参加物
実験手順
To a solution of 6.9 g (0.3 mole) of sodium pellets dissolved in 400 ml of absolute ethanol was successively added a solution of 37.9 g (0.305 mole) of guaiacol in 50 ml of ethanol followed by a solution of 68.1 g (0.35 mole) of diethylchloromalonate in 50 ml of ethanol. The mixture was heated at reflux for 28 hr and then stirred at ambient temperature for 3 days. The mixture was filtered and the filtrate was concentrated. The residue was partitioned between salt water and ethyl ether. The layers were separated and the aqueous layer was extracted twice with 150 ml portions of ethyl ether. The combined organic layers were washed with brine, dried (sodium sulfate0 and concentrated to give a yellow oil. The oil was subjected to vacuum distillation and 66.6 g (79%) of the title compound was collected as a clear oil, bp 136°-153° C. at 0.3 mm.
後処理
- temperatureThe mixture was heated
- temperatureat reflux for 28 hr
- filtrationThe mixture was filtered
- concentrationthe filtrate was concentrated
- customThe residue was partitioned between salt water and ethyl ether
- customThe layers were separated
- extractionthe aqueous layer was extracted twice with 150 ml portions of ethyl ether
- washThe combined organic layers were washed with brine
- dry with materialdried (sodium sulfate0
- concentrationconcentrated
- customto give a yellow oil
- distillationThe oil was subjected to vacuum distillation and 66.6 g (79%) of the title compound
- customwas collected as a clear oil, bp 136°-153° C. at 0.3 mm
出典と根拠
- ORDレコード
- ord-706d4735511c4c6da38794851e9015dd
- 出典データセット
- uspto-grants-1993_12
- 特許番号
- US05273993
関連ノート
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