Analyzing the synthesis route of 2199-44-2

This literature about this compound(2199-44-2)Product Details of 2199-44-2has given us a lot of inspiration, and I hope that the research on this compound(Ethyl 3,5-Dimethyl-2-pyrrolecarboxylate) can be further advanced. Maybe we can get more compounds in a similar way.

Product Details of 2199-44-2. The mechanism of aromatic electrophilic substitution of aromatic heterocycles is consistent with that of benzene. Compound: Ethyl 3,5-Dimethyl-2-pyrrolecarboxylate, is researched, Molecular C9H13NO2, CAS is 2199-44-2, about Electrophilic substitution of pyrroles with acyl chlorides. Author is Treibs, Alfred; Kreuzer, Franz H..

Pyrrole derivatives are readily substituted in the α and β positions by oxalyl chloride to give glyoxylic acid derivatives In the same way, pyrroles are substituted by trichloroacetyl chloride, in the absence of a catalyst, to give 2-trichloroacetylpyrroles, which afford pyrrolecarboxylic acids on treatment with alkali.

This literature about this compound(2199-44-2)Product Details of 2199-44-2has given us a lot of inspiration, and I hope that the research on this compound(Ethyl 3,5-Dimethyl-2-pyrrolecarboxylate) can be further advanced. Maybe we can get more compounds in a similar way.

Reference:
Thiazolidine – Wikipedia,
Thiazolidine – ScienceDirect.com