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 stirred solution of 4,4,6-Trimethyl-2-(3-nitro-phenyl)-1,2,3,4-tetrahydro-quinoline (10 g) in Ethanol/water (150 mL/30 mL) was added concentrated hydrochloric acid (2 mL) and Iron Powder (20 g, 356 mmol). The resultant mixture was heated to reflux for 2 h. Iron Powder was filtered, and washed with ethanol. The combined filtrate was concentrated, and diluted with water. The mixture was extracted with ethyl acetate (250 mL×3). The combined organic layers were washed with saturated brine, and the brine was extracted with ethyl acetate. The organic layers were dried over anhydrous sodium sulfate, concentrated. The residue was treated with ether and hexane to afford 4.5 g of 3-(4,4,6-trimethyl-1,2,3,4-tetrahydro-quinolin-2-yl)-phenylamine as brown solid (Yield: 50%).
WORKUP
后处理
- temperatureto reflux for 2 h
- filtrationIron Powder was filtered
- washwashed with ethanol
- concentrationThe combined filtrate was concentrated
- additiondiluted with water
- extractionThe mixture was extracted with ethyl acetate (250 mL×3)
- washThe combined organic layers were washed with saturated brine
- extractionthe brine was extracted with ethyl acetate
- dry with materialThe organic layers were dried over anhydrous sodium sulfate
- concentrationconcentrated
- additionThe residue was treated with ether and hexane