Extracurricular laboratory:new discovery of Ethyl 3-oxo-2,3-dihydrobenzofuran-2-carboxylate

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 13099-95-1

Electric Literature of 13099-95-1, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.13099-95-1, Name is Ethyl 3-oxo-2,3-dihydrobenzofuran-2-carboxylate, molecular formula is C11H10O4. In a Article£¬once mentioned of 13099-95-1

Synthesis of Basic Ethers of 3-Hydroxybenzofuro<2,3-c><1>benzopyran-6(H)-ones and 3-Hydroxynaphtho<1,2-b>furo<2,3-c><1>benzopyran-6(H)-ones

Synthesis of a number of 3-hydroxybenzofuro<2,3-c><1>benzopyran-6(H)-ones (IVa-g) and 3-hydroxynaphtho<1,2-b>furo<2,3-c><1>benzopyran-6(H)-ones (VIIa-f) has been carried out by the condensation of resorcinols with ethyl 2,3-dihydro-3-oxobenzofuran-2-carboxylate (III) and ethyl 2,3-dihydro-3-oxonaphtho<1,2-b>furan-2-carboxylate (VI), respectively in the presence of POCl3.Basic ethers (Va-v and VIIIa-l) of these compounds have been obtained by alkylation with beta-t-aminoalkyl halides in Me2CO-K2CO3.

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 13099-95-1

Reference£º
Benzofuran – Wikipedia,
Benzofuran | C8H3496O – PubChem