You Should Know Something about 2199-44-2

Compounds in my other articles are similar to this one(Ethyl 3,5-Dimethyl-2-pyrrolecarboxylate)Application In Synthesis of Ethyl 3,5-Dimethyl-2-pyrrolecarboxylate, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.

Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 2199-44-2, is researched, SMILESS is O=C(C1=C(C)C=C(C)N1)OCC, Molecular C9H13NO2Journal, Justus Liebigs Annalen der Chemie called Dithiocarboxylic acids of pyrroles. II. Friedel-Crafts reactions with carbon disulfide, Author is Treibs, Alfred; Friess, Raimund, the main research direction is pyrrole dithiocarboxylic acid preparation; dithiocarboxylic acid pyrrole preparation; Friedel Crafts reaction carbon disulfide; carbon disulfide Friedel Crafts reaction.Application In Synthesis of Ethyl 3,5-Dimethyl-2-pyrrolecarboxylate.

Reaction of 2,4-dimethyl-5-(ethoxycarbonyl)pyrrole (I) with AlCl3 in CS2 gave 10% 3-(dithiocarboxy) derivative (II) of I. The same reactions in the presence of ClCO2Et gave the Et ester of II. 2-Methyl-3-(ethoxycarbonyl)pyrrole-5-dithiocarboxylic acid was obtained in 10% yield from 2-methyl-3-(ethoxycarbonyl)pyrrole with AlCl3 and CS2. These reactions show CS2 was not an indifferent solvent in Friedel-Crafts reactions.

Compounds in my other articles are similar to this one(Ethyl 3,5-Dimethyl-2-pyrrolecarboxylate)Application In Synthesis of Ethyl 3,5-Dimethyl-2-pyrrolecarboxylate, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.

Reference:
Thiazolidine – Wikipedia,
Thiazolidine – ScienceDirect.com