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
To a solution of 4-hydroxybenzaldehyde (4.04 g, 33.08 mmol), in acetonitrile (50 ml) was added K2CO3 (10.1 g), followed by N-(2-chloroethyl)morpholine hydrochloride (6.16 g). The reaction mixture was heated to reflux overnight, additional N-(2-chloroethyl)morpholine hydrochloride (0.6 g) and K2CO3 (0.5 g) were added and the mixture was refluxed for another 3 hours. The reaction mixture was cooled to room temperature, filtered, and the filtrate was treated with DARCO®, filtered and the solvent was stripped. The residue was partitioned between saturated NaHCO3 (150 ml) and ethyl acetate (300 ml). The layers were separated and the organic layer was washed with 1N NaOH, dried over MgSO4, filtered and stripped to afford, as an amber oil, 6.41 g of 4-[2-(4-morpholinyl)ethoxy]benzaldehyde.
WORKUP
后处理
- temperatureThe reaction mixture was heated
- temperatureto reflux overnight
- temperaturethe mixture was refluxed for another 3 hours
- filtrationfiltered
- additionthe filtrate was treated with DARCO®
- filtrationfiltered
- customThe residue was partitioned between saturated NaHCO3 (150 ml) and ethyl acetate (300 ml)
- customThe layers were separated
- washthe organic layer was washed with 1N NaOH
- dry with materialdried over MgSO4
- filtrationfiltered