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HRID1787373

反应详情

EQUATION

反应方程式

HRID 1787373 的结构方程式

REACTANTS

反应物

2
结构：Nc1ccccc1OC(F)(F)F
HCID73754

2-(Trifluoromethoxy)aniline

C7H6F3NO

结构：Cc1c(NC(=O)CC(C)(C)C)cc2c(c1C)OC(C)(C)C2O
HCID23114263

未命名化合物

PRODUCTS

生成物

1
结构：Cc1c(NC(=O)CC(C)(C)C)cc2c(c1C)OC(C)(C)C2Nc1ccccc1OC(F)(F)F
HCID23114247

未命名化合物

收率 73%

AUXILIARIES

试剂、催化剂与溶剂

1
结构：CCCCCC.CCOC(C)=O
溶剂HCID21226206

未命名化合物

PROCEDURE

实验过程

Using N-(3-hydroxy-2,2,6,7-tetramethyl-2,3-dihydro-1-benzofuran-5-yl)-3,3-dimethylbutanamide obtained in Example 235 and (2-(trifluoromethoxy)phenyl)amine, the title compound was synthesized in the same manner as in Example 297. Yield: 73%. Melting point: 196-197° C. (ethyl acetate-hexane).