Реакция #323068

Уравнение реакции

2-[2-(4-chlorophenyl)-5-(2-furyl)-4-oxazolyl]acetic acid

2-chloro-1-methylpyridinium iodide

laurylalcohol

triethylamine

→

lauryl 2-[2-(4-chlorophenyl)-5-(2-furyl)-4-oxazolyl]acetate

Выход 77.4%

Растворители

tetrahydrofuran

Условия реакции

Методика

2.0 g of 2-[2-(4-chlorophenyl)-5-(2-furyl)-4-oxazolyl]acetic acid, 2.02 g of 2-chloro-1-methylpyridinium iodide, 1.47 g of laurylalcohol, 1.60 g of triethylamine and 60 ml of tetrahydrofuran are treated in the same manner as described in Example 27. 2.4 g of lauryl 2-[2-(4-chlorophenyl)-5-(2-furyl)-4-oxazolyl]acetate are obtained. Yield: 77.4%

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