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 solution of biphenyl-4-ylamine (150 mg, 0.883 mmoles) and 4-formyl-5-methyl-furan-2-carboxylic acid methyl ester (157) (135 mg, 0.803 mmoles) in methanol (2.0 ml) was stirred over molecular sieves (type 3 Å) for 1 hour. Sodium cyanoborohydride (55 mg, 0.883 mmoles) was added and the mixture stirred for 18 hour at room temperature. The mixture was concentrated and partitioned between ethyl acetate (25 ml) and saturated aqueous sodium bicarbonate (30 ml). The aqueous phase was re-extracted with ethyl acetate (2×25 ml) and the combined extracts were washed with brine (50 ml) and dried (MgSO4). After removal of the solvent, the residue was purified by flash chromatography, using a gradient elution of petrol/diethyl ether 9:1 v/v to 4:1 v/v, to afford compound 158 (75 mg).
WORKUP
后处理
- concentrationThe mixture was concentrated
- custompartitioned between ethyl acetate (25 ml) and saturated aqueous sodium bicarbonate (30 ml)
- extractionThe aqueous phase was re-extracted with ethyl acetate (2×25 ml)
- washthe combined extracts were washed with brine (50 ml)
- dry with materialdried (MgSO4)
- customAfter removal of the solvent
- customthe residue was purified by flash chromatography
- washa gradient elution of petrol/diethyl ether 9:1 v/v to 4:1 v/v