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
- 20 °C
PROCEDURE
实验过程
7-Hydroxy-5,6-dihydro-4H-dibenzo[de,h]quinoline (27 g) [prepared as described in Example 2] is added to a suspension of sodium hydride (50% dispersion in mineral oil; (5.75 g) in anhydrous dimethylformamide (520 cc) and then, after stirring for 4 hours, ethyl bromoacetate (21.3 g) in solution in anhydrous dimethylformamide (20 cc) is added. The reaction mixture is maintained for 22 and a half hours at about 20° C., is distilled water (10 cc) is added, the mixture is concentrated to a volume of 400 cc, distilled water (4600 cc) is added and the mixture is extracted eight times with diethyl ether (total 3500 cc). The combined organic solutions are washed four times with distilled water (total 4000 cc), dried over anhydrous sodium sulphate, treated with decolourising charcoal (5 g), filtered and evaporated to dryness. The residue is dried by azeotropic distillation with methylene chloride (150 cc) and then crystallised from ethanol (16 cc). After cooling for 21 hours at about 5° C., the resulting crystals are filtered off, washed twice with ethanol (total 18 cc), which has been cooled to -20° C., and dried under reduced pressure (20 mm Hg) at 20° C. Ethyl (5,6-dihydro-4H-dibenzo[de,h]quinol-7-yloxy)acetate (16.95 g), melting at 70° C., is thus obtained.
WORKUP
后处理
- distillationis distilled water (10 cc)
- additionis added
- concentrationthe mixture is concentrated to a volume of 400 cc
- distillationdistilled water (4600 cc)
- additionis added
- extractionthe mixture is extracted eight times with diethyl ether (total 3500 cc)
- washThe combined organic solutions are washed four times with distilled water (total 4000 cc)
- dry with materialdried over anhydrous sodium sulphate
- additiontreated with decolourising charcoal (5 g)
- filtrationfiltered
- customevaporated to dryness
- dry with materialThe residue is dried by azeotropic distillation with methylene chloride (150 cc)
- customcrystallised from ethanol (16 cc)
- temperatureAfter cooling for 21 hours at about 5° C.
- filtrationthe resulting crystals are filtered off
- washwashed twice with ethanol (total 18 cc), which
- temperaturehas been cooled to -20° C.
- customdried under reduced pressure (20 mm Hg) at 20° C