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HRID515871

反应详情

EQUATION

反应方程式

HRID 515871 的结构方程式

REACTANTS

反应物

4
结构：O=Cc1cc2c(cc1Br)OCO2
HCID95062

1,3-Benzodioxole-5-carboxaldehyde, 6-bromo- (9CI)

C8H5BrO3

结构：CCOC(=O)c1cc[nH]c1C
HCID136747

2-Methyl-1H-pyrrole-3-carboxylic acid ethyl ester

C8H11NO2

结构：O=Cc1ccc(Cl)cc1Br
HCID13154710

2-Bromo-4-chlorobenzaldehyde

C7H4BrClO

结构：CCOC(=O)c1cc[nH]c1C(F)(F)F
HCID85684081

未命名化合物

PRODUCTS

生成物

1
结构：CCOC(=O)c1cc(-c2cc3c(cc2C(=O)O)OCO3)n(C)c1C(F)(F)F
HCID117833890

未命名化合物

PROCEDURE

实验过程

The procedure is in accordance with the process of Preparation 1, replacing in Step A the ethyl 2-methyl-1H-pyrrole-3-carboxylate by ethyl 2-(trifluoromethyl)-1H-pyrrole-3-carboxylate and also the 2-bromo-4-chlorobenzaldehyde used in Step B by 6-bromo-1,3-benzodioxole-5-carbaldehyde.

WORKUP

后处理

  1. customThe procedure is in accordance with the process of Preparation 1