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
CONDITIONS
反应条件
- 温度
- 0 °C
PROCEDURE
实验过程
A mixture of Z-(1H-Pyrrol-2-ylmethylene)-1,3-dihydro-indol-2-one (120 mg, 0.57 mmol), paraformaldehyde (17 mg, 0.57 mmol), and 1-methylpiperazine (63 μL, 0.57 mmol) in 4.0 mL EtOH was heated at reflux for 6.5 h. After standing at room temperature for 23 h, the mixture was concentrated to 3 mL solvent and 1 mL of hexane added. The resulting solution was cooled to 0° C. and the yellow solid which formed was collected by filtration. The solid collected was partitioned between 30 mL dilute HCl and 20 mL Ethyl acetate. The organic layer was removed and the aqueous layer washed with ethyl acetate (15 mL). The aqueous layer was made basic to pH 8 with saturated NaHCO3 and extracted with ethyl acetate. The ethyl acetate layer was washed with H2O, brine and dried with Na2SO4. The organic layer was concentrated and the residue was crystallized from ethyl acetate/hexane to give the title compound (38 mg, 21%) as a bright yellow solid.
WORKUP
后处理
- temperaturewas heated
- temperatureat reflux for 6.5 h
- concentrationthe mixture was concentrated to 3 mL solvent and 1 mL of hexane
- additionadded
- customthe yellow solid which formed
- filtrationwas collected by filtration
- customThe solid collected
- customwas partitioned between 30 mL dilute HCl and 20 mL Ethyl acetate
- customThe organic layer was removed
- washthe aqueous layer washed with ethyl acetate (15 mL)
- extractionextracted with ethyl acetate
- washThe ethyl acetate layer was washed with H2O, brine
- dry with materialdried with Na2SO4
- concentrationThe organic layer was concentrated
- customthe residue was crystallized from ethyl acetate/hexane