Process for producing 4-phenyl-4-oxo-2-butenoic ester derivative
View Patent ↗A 4-phenyl-4-oxo-2-butenoate derivative is stably supplied in a short period of time, at low cost, in high purity and on an industrial scale by a process for producing the 4-phenyl-4-oxo-2-butenoate derivative, which comprises simultaneously or continuously reacting a sulfuric ester, an aromatic hydrocarbon and a maleic anhydride derivative.
1. A process for producing a 4-phenyl-4-oxo-2-butenoate derivative represented by the following general formula (III) or (IV), which comprises simultaneously or continuously reacting an aromatic hydrocarbon represented by the following general formula (I) and a maleic anhydride derivative represented by the following general formula (II) in the presence of an acid catalyst and an alkylating agent wherein the alkylating agent is a sulfuric ester
wherein R1 to R5 each independently represents a hydrogen atom, an electron-donating group, or an electron-withdrawing group, and adjacent groups of R1 to R5 may be combined to form a ring;
wherein R6 or R7 each independently represents a hydrogen atom, an alkyl group, an alkenyl group, an alkynyl group, an aryl group, an alkoxy group, an aryloxy group, a carbonyl group, a sulfonyl group, a carbonyloxy group, a carbonylamino group, a sulfonylamino group, an amino group, a cyano group, an alkylthio group, an arylthio group, a heterocyclic residual group, or a halogen atom, and R6 and R7 may be combined to form a partially saturated ring, an aromatic ring, or a heterocyle;
wherein R1 to R7 have the same meanings as above and R8 represents an alkyl group.
2. The process for producing the 4-phenyl-4-oxo-2-butenoate derivative according to claim 1 , wherein R1 to R5 in the above general formula (I) each independently is a hydrogen atom or an electron-donating group.
3. The process for producing the 4-phenyl-4-oxo-2-butenoate derivative according to claim 1 , wherein the above general formula (I) has at least one electron-donating group and at least one electron-withdrawing group, and the total of Hammett's substituent constant σ values of R1 to R5 is 0 or more.
4. The process for producing the 4-phenyl-4-oxo-2-butenoate derivative according to claim 1 , wherein the electron-donating group of R1 to R5 in the above general formula (I) is a group chosen from alkoxy, alkylthio, monosubstituted amino, and disubstituted amino.
5. The process for producing the 4-phenyl-4-oxo-2-butenoate derivative according to claim 1 , wherein the acid catalyst is aluminum chloride.
6. The process for producing the 4-phenyl-4-oxo-2-butenoate derivative according to claim 1 , which is used for producing a 4-phenyl-2-butene-1,4-dione derivative represented by the following general formula (V) or (VI):
wherein R1 to R7 have the same meanings as above and R9 represents a hydrogen atom, an alkyl group, an aryl group, a hydroxyl group, an amino group, or a hydroxylamino group.