反应 #96089

ord-1410d8e26cce40e88ea0a306d2e1de5d

反应条件

温度
0°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONUpon complete addition the reaction mixture
  2. 2
    温度to warm to ambient temperature
  3. 3
    workup.STIRRINGwith stirring for one hour
  4. 4
    其他the layers separated
  5. 5
    洗涤the aqueous layer washed with two portions of 250 ml each of diethyl ether
  6. 6
    洗涤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. 7
    干燥The organic layer was dried with magnesium sulfate
  8. 8
    过滤filtered
  9. 9
    浓缩the filtrate concentrated under reduced pressure to an oil residue
  10. 10
    workup.DISTILLATIONThe oil was distilled under reduced pressure

实验过程

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.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US04346251uspto-grants-1982_08