反应 #1265367

ord-dfb80ab567c9463587071e3d25f3bfa6

反应方程式

c1ccc2[nH]cnc2c1
benzimidazole
COc1ccc(C(=O)OCCCl)cc1
2-chloroethyl 4-methoxybenzoate
COc1ccc(C(=O)OCCn2c(-c3ccccc3)nc3ccccc32)cc1
2-(2-phenyl-1H-benzimidazol-1-yl)ethyl 4-methoxybenzoate
收率 71.0%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The procedure of Synthesis Example 10

实验过程

The procedure of Synthesis Example 10 was repeated except that benzimidazole was used instead of the 1-aza-18-crown-6, and 2-chloroethyl 4-methoxybenzoate was used instead of the 2-chloroethyl benzoate, to give 2-(2-phenyl-1H-benzimidazol-1-yl)ethyl 4-methoxybenzoate in a yield of 71%.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07276324B2uspto-grants-2007_10