Реакция #81152

Уравнение реакции

dimethyl 2-butylimidazole-4,5-dicarboxylate

t-butyl 4'-bromomethylbiphenyl-2-carboxylate

sodium methoxide

sodium

→

title compound

Выход 99.5%

Dimethyl 1-[(2'-t-butoxycarbonylbiphenyl-4yl)methyl]-2-butylimidazole-4,5-dicarboxylate

Выход 99.5%

Растворители

water

ethyl acetate

methanol

N,N-dimethylacetamide

N,N-dimethylacetamide

methanol

Условия реакции

Обработка

1. 1
   Концентрированиеthe resulting mixture was concentrated by evaporation under reduced pressure
2. 2
   workup.ADDITIONThe resulting residue was mixed with benzene
3. 3
   Концентрированиеthe mixture was concentrated by distillation under reduced pressure
4. 4
   Другоеthe solid thus obtained
5. 5
   Другоеthe ethyl acetate layer was separated
6. 6
   Сушкаdried over anhydrous magnesium sulfate
7. 7
   Другоеthe solvent was then removed by distillation under reduced pressure
8. 8
   ДругоеThe residue was purified by column chromatography through silica gel
9. 9
   workup.ADDITIONby volume mixture of ethyl acetate and hexane as the eluent

Методика

A sodium methoxide solution prepared from 0.69 g of sodium and 40 ml of methanol was added to a solution of 7.2 g of dimethyl 2-butylimidazole-4,5-dicarboxylate (prepared as described in Preparation 4) in 40 ml of methanol, and the resulting mixture was concentrated by evaporation under reduced pressure. The resulting residue was mixed with benzene, and the mixture was concentrated by distillation under reduced pressure. After this operation had been repeated three times, the solid thus obtained was dissolved in 72 ml of N,N-dimethylacetamide. A solution of 10.41 g of t-butyl 4'-bromomethylbiphenyl-2-carboxylate in 100 ml of N,N-dimethylacetamide was then added dropwise to the resulting solution. The reaction mixture was then stirred at room temperature for 1 hour and at 50°-55° C. for 2 hours. At the end of this time, it was mixed with ethyl acetate and water, and the ethyl acetate layer was separated, and dried over anhydrous magnesium sulfate; the solvent was then removed by distillation under reduced pressure. The residue was purified by column chromatography through silica gel, using a 1:1 by volume mixture of ethyl acetate and hexane as the eluent, to give 15.1 g of the title compound as a gum.

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