HRID1036401

反应详情

EQUATION

反应方程式

HRID 1036401 的结构方程式

PROCEDURE

实验过程

(R)-4-(6-Hydroxynaphthalen-2-yl)-4-methyl-oxazolidin-2-one (Example 4, 0.301 g, 0.00124 mol) was dissolved in tetrahydrofuran (5.00 mL, 0.0616 mol). 4-Propylcyclohexanol (0.211 g, 0.00148 mol) and triphenylphosphine polymer-bound (1.07 g, 0.00198 mol) were added and the mixture was stirred at room temperature. Diisopropyl azodicarboxylate (0.390 mL, 0.00198 mol) was then added and the mixture was stirred for 2 days at room temperature. The mixture was filtered through CELITE™, concentrated and purified by flash chromatography (0-30% EtOAc in methylene chloride) to give 0.4942 g of the title product (109% yield).

WORKUP

后处理

  1. stirringthe mixture was stirred for 2 days at room temperature
  2. filtrationThe mixture was filtered through CELITE™
  3. concentrationconcentrated
  4. custompurified by flash chromatography (0-30% EtOAc in methylene chloride)