HRID514155

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：CCOC(=O)C(O)c1c(C)cc2ccc(Cl)cc2c1-c1ccc(Cl)cc1

HCID67126265

未命名化合物

结构：CCOC(=O)[C@@H](OC(C)(C)C)c1c(C)cc2cc(OS(=O)(=O)C(F)(F)F)ccc2c1-c1ccc(Cl)cc1

HCID86691548

未命名化合物

PRODUCTS

生成物

结构：CCOC(=O)C(OC(C)(C)C)c1c(C)cc2ccc(Cl)cc2c1-c1ccc(Cl)cc1

HCID67126236

未命名化合物

PROCEDURE

实验过程

Ethyl 2-tert-butoxy-2-(7-chloro-1-(4-chlorophenyl)-3-methylnaphthalen-2-yl)acetate was prepared in a manner similar to (S)-ethyl 2-tert-butoxy-2-(1-(4-chlorophenyl)-3-methyl-6-(trifluoromethylsulfonyl-oxy)naphthalen-2-yl)acetate of Example 51, except using racemic ethyl 2-(7-chloro-1-(4-chlorophenyl)-3-methylnaphthalen-2-yl)-2-hydroxyacetate. Material was carried on crude without further characterization.