HRID1284118
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 mixture of 5.0 g. of 3-hydroxymethylene-6,7-dimethoxy-2-methyl-4-oxo-1,2,3,4-tetrahydro-1-quinoline carboxylic acid, benzyl ester and 5.0 g. of ammonium acetate in 200 ml. of ethanol is heated to reflux for 35 min. The reaction mixture is concentrated to dryness and the residue taken up in 200 ml. of chloroform. The chloroform solution is then washed successively with water (1 × 100 ml.), 1N aqueous sodium hydroxide (2 × 100 ml.) and brine (1 × 100 ml.), dried over magnesium sulfate and concentrated to dryness. The residual oil is crystallized from ethyl acetate, 3.34 g., m.p. 143°-149.5°C. and 1.3 g. recrystallized from the same solvent, 660 mg., m.p. 144°-146.5°C.
WORKUP
后处理
- additionA mixture of 5.0 g
- temperatureto reflux for 35 min
- concentrationThe reaction mixture is concentrated to dryness
- washThe chloroform solution is then washed successively with water (1 × 100 ml.), 1N aqueous sodium hydroxide (2 × 100 ml.) and brine (1 × 100 ml.)
- dry with materialdried over magnesium sulfate
- concentrationconcentrated to dryness
- customThe residual oil is crystallized from ethyl acetate, 3.34 g
- customrecrystallized from the same solvent, 660 mg