HRID2213160
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
A suspension was prepared of 47 g (167 mmol) of 2-(3-methoxyphenyl)-6-methoxy-1-tetralone and 4.7 g of p-toluenesulfonic acid mono-hydrate in 470 mL of iso-propenylacetate. The reaction mixture was refluxed for forty-eight hours under a nitrogen atmosphere. The reaction was allowed to cool and 10 g of NaHCO3 was added the solution was poured into 500 mL of an aqueous solution of NaHCO3. The aqueous solution was extracted three times with 200 mL portions of EtOAc. The combined organic extract was washed with brine, dried with Na2SO4, and evaporated to a dark oil. This yielded 52.7 g of the title compound.
WORKUP
后处理
- temperatureThe reaction mixture was refluxed for forty-eight hours under a nitrogen atmosphere
- temperatureto cool
- extractionThe aqueous solution was extracted three times with 200 mL portions of EtOAc
- extractionThe combined organic extract
- washwas washed with brine
- dry with materialdried with Na2SO4
- customevaporated to a dark oil