反応 #96089
ord-1410d8e26cce40e88ea0a306d2e1de5d
反応方程式
反応条件
後処理
- 1workup.ADDITIONUpon complete addition the reaction mixture
- 2温度to warm to ambient temperature
- 3workup.STIRRINGwith stirring for one hour
- 4その他the layers separated
- 5洗浄the aqueous layer washed with two portions of 250 ml each of diethyl ether
- 6洗浄the whole was washed with one portion of 500 ml of aqueous 5% hydrochloric acid, one portion of 500 ml of water, one portion of 300 ml of a solution saturated with sodium bicarbonate
- 7乾燥The organic layer was dried with magnesium sulfate
- 8ろ過filtered
- 9濃縮the filtrate concentrated under reduced pressure to an oil residue
- 10workup.DISTILLATIONThe oil was distilled under reduced pressure
実験手順
A stirred mixture of 12.5 g (0.54 mole) of sodium hydride (25 g of a 50% dispersion in mineral oil) in 300 ml of dimethylformamide and 900 ml of benzene was placed under a nitrogen atmosphere and cooled to 0° C. To this mixture, 104.3 g (0.9 moles) of diethyl malonate was added dropwise during a 5 minute period and the mixture was stirred until hydrogen evolution ceased. 2-(Bromomethyl)biphenyl (117 g, 0.47 mole) was then added at 0° C. Upon complete addition the reaction mixture was stirred at 0° C. for 30 minutes, then was allowed to warm to ambient temperature with stirring for one hour. The reaction mixture was poured into 500 ml of water, the layers separated, and the aqueous layer washed with two portions of 250 ml each of diethyl ether. The organic layer was combined with the ether washings, and the whole was washed with one portion of 500 ml of aqueous 5% hydrochloric acid, one portion of 500 ml of water, one portion of 300 ml of a solution saturated with sodium bicarbonate, and finally, one portion of 500 ml of water. The organic layer was dried with magnesium sulfate, filtered, and the filtrate concentrated under reduced pressure to an oil residue. The oil was distilled under reduced pressure to give 149.0 g of diethyl (2-phenylbenzyl)malonate; b.p. 175°-180° C./0.8-0.9 mm. The nmr spectrum was consistent with the proposed structure.