Archives for Chemistry Experiments 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, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.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

The synthesis of ethyl 3-hydroxybenzofuro<3,2-b>furan-2-carboxylate (3a), 2-acetyl-3-hydroxybenzofuro<3,2-b>furan (3b) and 3-hydroxybenzofuro<3,2-b>furan-2-carbonitrile (3c) from 2-carbethoxy-3(2H)-benzofuranone (1) by condensation with ethyl bromoacetate, chloracetone and chloroacetonitrile and subsequent Dieckmann cyclisation is reported.Reaction of 1 with aromatic amines under different reaction conditiones have also been investigated.

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：
Benzofuran – Wikipedia,
Benzofuran | C8H3511O – PubChem