HRID71224

反应详情

EQUATION

反应方程式

HRID 71224 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

Nitrogen was bubbled in a solution of 4-hydroxy-3,5-dimethylbenzonitrile (5.0 g, 34.0 mmol) and (R)-(−)-2,2-dimethyl-1,3-dioxolane-4-methanol (9.53 ml, 76 mmol) in THF (125 ml) at room temperature. The solution was made in a 500 ml flask w/3 necks fitted with a reflux condenser for 10 min. To this was added triphenylphosphine (20.05 g, 76 mmol) in one portion. Nitrogen was bubbled for an additional 10 minutes, followed by the dropwise addition of diethyl azodicarboxylate (12.04 ml, 76 mmol). The color of the reaction mixture changed from pale to a dark reddish brown and the reaction was exothermic. The reaction vessel was immersed in a preheated oil bath held at 65° C. The reaction was found to be nearly complete after 3 h. The contents of the reactor were cooled and evaporated. The semi solid residue was taken in ether and washed with water. The aqueous layer was extracted with ether (2×). The combined organic layer was then washed with brine. It was then dried over anhydrous MgSO4., and then concentrated. Triphenylphosphineoxide was crystallized out and filtered with ether and hexanes. The product was purified on a 330 g ISCo cartridge eluted with 0 to 30% EtOAc-hexanes. (R)-4-((2,2-dimethyl-1,3-dioxolan-4-yl)methoxy)-3,5-dimethylbenzonitrile (7.49 g, 28.7 mmol, 84% yield) was obtained as a clear oil. 1H NMR (400 MHz, CCl3D) δ ppm 7.27 (2H, s), 4.38-4.49 (1H, m), 4.08-4.19 (1H, m), 3.88 (1H, ddd, J=8.18, 5.99, 1.87 Hz), 3.73-3.84 (2H, m), 2.25 (6H, s), 1.41 (3H, s), 1.36 (3H, s).

WORKUP

后处理

  1. customThe solution was made in a 500 ml flask
  2. customw/3 necks fitted with a reflux condenser for 10 min
  3. customNitrogen was bubbled for an additional 10 minutes
  4. customThe reaction vessel was immersed in a preheated oil bath
  5. customheld at 65° C
  6. temperatureThe contents of the reactor were cooled
  7. customevaporated
  8. washwashed with water
  9. extractionThe aqueous layer was extracted with ether (2×)
  10. washThe combined organic layer was then washed with brine
  11. dry with materialIt was then dried over anhydrous MgSO4
  12. concentration, and then concentrated
  13. customTriphenylphosphineoxide was crystallized out
  14. filtrationfiltered with ether and hexanes
  15. customThe product was purified on a 330 g ISCo cartridge
  16. washeluted with 0 to 30% EtOAc-hexanes