HRID1727001

反应详情

EQUATION

反应方程式

HRID 1727001 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A mixture of 2 g (8 mmol) of 4-benzyloxy-naphthalen-1-ol [Journal of Medicinal Chemistry (1985), 28(6), 822-41, of 2.67 g (16 mmol) of ethyl bromoacetate and of 3.12 g (9.6 mmol) of cesium carbonate in 30 ml of acetonitrile was stirred at 60° C. for 3 hours. Subsequently, the reaction mixture was evaporated to dryness and the residue was partitioned between water and tert.-butyl methyl ether. The organic phase was separated, washed with water and brine, dried over anhydrous sodium sulfate and finally evaporated. 2.23 g of the title compound were obtained as white crystals after crystallization from n-heptane.

WORKUP

后处理

  1. customSubsequently, the reaction mixture was evaporated to dryness
  2. customthe residue was partitioned between water and tert.-butyl methyl ether
  3. customThe organic phase was separated
  4. washwashed with water and brine
  5. dry with materialdried over anhydrous sodium sulfate
  6. customfinally evaporated