HRID1110224

反应详情

EQUATION

反应方程式

HRID 1110224 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a suspension of 5.0 g (10.85 mmol) of 3,5-bis[(1-oxodecyl)amino]benzoic acid in 150 ml of anhydrous toluene cooled in an ice bath and stirred under an argon atmosphere was added 2.8 ml (13.0 mmol) of diphenylphosphoryl azide followed by 1.8 ml (13.0 mmol) of triethylamine. The reaction mixture was stirred in the ice bath for 1.5 hours, at room temperature for 1 hour and then at 90° C. for 2 hours. Benzyl alcohol (39 ml, 0.38 mol) was added and heating at 90° was continued for 4 hours. The solvent was removed at reduced pressure and most of the excess benzyl alcohol was removed at 80°/1 mm. NaHCO3 solution was added and the product was extracted with ethyl acetate. The dried extract was concentrated at reduced pressure and the residue was purified by HPLC using 25% ethyl acetate-hexane to give 27.8 g (45% yield) of [3,5-bis[(1-oxodecyl)amino]phenyl]carbamic acid phenylmethyl ester as a yellow foam. The nmr and mass spectra were compatible with the structure.

WORKUP

后处理

  1. temperaturecooled in an ice bath
  2. temperatureheating at 90°
  3. waitwas continued for 4 hours
  4. customThe solvent was removed at reduced pressure and most of the excess benzyl alcohol
  5. customwas removed at 80°/1 mm
  6. additionNaHCO3 solution was added
  7. extractionthe product was extracted with ethyl acetate
  8. extractionThe dried extract
  9. concentrationwas concentrated at reduced pressure
  10. customthe residue was purified by HPLC