HRID355761

反应详情

EQUATION

反应方程式

HRID 355761 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-70 °C

PROCEDURE

实验过程

A mixture of 2-phenethyl benzoic acid (11.3 g), oxalyl chloride (5.2 ml), DMF (0.2 ml) and dichloromethane (100 ml) was stirred for 1.5 hours. The solvent was evaporated, diglyme (75 ml) added and the mixture cooled to -70° C. Lithium tri-(tert-butoxy)aluminium hydride (100 ml, 0.5M solution in diglyme) was added dropwise over 45 minutes maintaining the reaction temperature below -60° C. The reaction was stirred at -70° C. for 1 hour and poured into a 2N HCl and ice mixture. The mixture was extracted with iso-hexane (3×100 ml). The extracts were washed with saturated aqueous sodium hydrogen carbonate, water and brine, dried (MgSO4), filtered and evaporated. The residue was purfied by MPLC eluting with dichloromethane/iso-hexane (1:1) to give 2-(phenethyl)benzaldehyde (7.77 g).

WORKUP

后处理

  1. customThe solvent was evaporated
  2. additiondiglyme (75 ml) added
  3. additionLithium tri-(tert-butoxy)aluminium hydride (100 ml, 0.5M solution in diglyme) was added dropwise over 45 minutes
  4. temperaturemaintaining the reaction temperature below -60° C
  5. stirringThe reaction was stirred at -70° C. for 1 hour
  6. additionpoured into a 2N HCl and ice mixture
  7. extractionThe mixture was extracted with iso-hexane (3×100 ml)
  8. washThe extracts were washed with saturated aqueous sodium hydrogen carbonate, water and brine
  9. dry with materialdried (MgSO4)
  10. filtrationfiltered
  11. customevaporated
  12. washeluting with dichloromethane/iso-hexane (1:1)