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
In a closed system equipped with a Dean-Stark trap, a stirred solution of 4,4-dichlorobenzoin (10.0 g, 0.0357 mole), ethanolamine (2.35 g, 0.0385 mole), and a catalytic amount of p-toluenesulfonic aid in 250 ml toluene was heated at reflux temperature for 4 hours and the azeotroped water was collected in the Dean-Stark trap. After cooling, the toluene solution was washed with water, dried over magnesium sulfate and concentrated to an oil. The oil was dissolved in ether, treated with excess ethereal hydrogen chloride and the salt collected under nitrogen. Upon trying to recrystallize the salt from 350 ml of isopropyl ether (necessary for complete solution), 500 ml isopropyl ether, a yellow solid was obtained from this solution which was identified as 4,4'-dichlorobenzil. The filtrate was concentrated to 50 ml and isopropyl ether added to the hot solution until a faint turbidity was obtained. On standing overnight, a white solid was obtained, m.p. 177°-182° C. Recrystallization of the white solid from methanol-isopropyl ether and from acetonitrile-methanol yielded only semisolid salts. These were triturated with methyl ethyl ketone and dried to give 2.04 g total, m.p. 188°-193° C. This material gave a satisfactory elemental analysis for the title compound.
WORKUP
后处理
- customIn a closed system equipped with a Dean-Stark trap
- temperatureat reflux temperature for 4 hours
- customthe azeotroped water was collected in the Dean-Stark trap
- temperatureAfter cooling
- washthe toluene solution was washed with water
- dry with materialdried over magnesium sulfate
- concentrationconcentrated to an oil
- dissolutionThe oil was dissolved in ether
- additiontreated with excess ethereal hydrogen chloride
- customthe salt collected under nitrogen
- customto recrystallize the salt from 350 ml of isopropyl ether (necessary for complete solution), 500 ml isopropyl ether
- customa yellow solid was obtained from this solution which
- concentrationThe filtrate was concentrated to 50 ml and isopropyl ether
- additionadded to the hot solution until a faint turbidity
- customwas obtained
- customa white solid was obtained
- customRecrystallization of the white solid from methanol-isopropyl ether
- customfrom acetonitrile-methanol yielded only semisolid salts
- customThese were triturated with methyl ethyl ketone
- customdried
- customto give 2.04 g total