Method for producing phenolphthalein compound using ionic liquid catalyst composition
View Patent ↗A method for producing a phenolphthalein compound is disclosed, comprising: reacting a phenolic compound of the formula: wherein R a is a hydrogen or a C 1 -C 12 hydrocarbyl group, with a phthalic anhydride compound of the formula: wherein R b is a hydrogen, a C 1 -C 12 hydrocarbyl group, or a halogen, in the presence of an ionic liquid catalyst composition and a promoter to form a reaction mixture comprising a phenolphthalein compound of the formula: wherein each R a is independently a hydrogen or a C 1 -C 12 hydrocarbyl group, and R b is a hydrogen, a C 1 -C 12 hydrocarbyl group, or a halogen; wherein the ionic liquid catalyst composition comprises a combination of an ionic liquid and a metal halide wherein the metal is selected from the group consisting of a Group IIB, IIIA, VIII, or IVA metal, and a combination thereof.
1. A method for producing a phenolphthalein compound
comprising:
reacting a phenolic compound of the formula:
wherein R a is a hydrogen or a C 1 -C 12 hydrocarbyl group, with a phthalic anhydride compound of the formula:
wherein R b is a hydrogen, a C 1 -C 12 hydrocarbyl group, or a halogen, in the presence of an ionic liquid catalyst composition and a promoter to form a reaction mixture comprising a phenolphthalein compound of the formula:
wherein each R a is independently a hydrogen or a C 1 -C 12 hydrocarbyl group, and R b is a hydrogen, a C 1 -C 12 hydrocarbyl group, or a halogen;
wherein the ionic liquid catalyst composition comprises a combination of an ionic liquid and a metal halide wherein the metal is selected from the group consisting of a Group IIB, IIIA, VIII, or IVA metal, and a combination thereof.
2. The method of claim 1 wherein the ionic liquid is a quaternary organic ammonium salt that is a liquid at 25° C.
3. The method of claim 1 wherein the ionic liquid is an imidazolium salt, pyrazolium salt, pyridinium salt, pyrimidinium salt, pyrazinium salt, C 1 -C 32 tetraalkyl ammonium salt, C 1 -C 32 tetraalkyl phosphonium salt, or a combination comprising at least one of the foregoing salts, wherein each of the foregoing salts is a liquid at 25° C.
4. The method of claim 1 wherein the ionic liquid is:
a salt of the formula:
wherein R 1 and R 5 are independently a C 1 -C 8 hydrocarbyl group, R 2 , R 3 , and R 4 are each independently a hydrogen or a C 1 -C 8 hydrocarbyl group, and X − is anion;
a salt of the formula:
wherein R 6 is a C 1 -C 8 hydrocarbyl, R 7 , R 8 , and R 9 are each independently a hydrogen atom or a C 1 -C 8 hydrocarbyl group, and X − is an anion;
a salt of the formula:
wherein R 11 is a C 1 -C 8 hydrocarbyl group, each R 10 is independently a hydrogen or a C 1 -C 8 hydrocarbyl group, and X − is an anion;
a salt of the formula:
wherein R 12 is a C 1 -C 8 hydrocarbyl group, each R 13 is independently a hydrogen or C 1 -C 8 hydrocarbyl group, n is 1 to 4, and X − is an anion,
a salt of the formula:
wherein R 14 , R 15 , R 16 , and R 17 are each independently a C 1 -C 8 hydrocarbyl group, and X − is an anion; or
a combination comprising at least one of the foregoing salts.
5. The method of claim 4 wherein X − in each salt is independently a fluoride, bromide, or chloride.
6. The method of claim 1 wherein the ionic liquid is a 1,3-alkylimidazolium salt, a N-alkyl pyridinium salt, or a combination comprising at least one of the foregoing salts, wherein each alkyl independently has 1 to 6 carbon atoms.
7. The method of claim 1 wherein the molar ratio of the ionic liquid to the metal halide is 1:1 to 1:3.
8. The method of claim 1 wherein the molar ratio of the ionic liquid to the metal halide is 1:1.8 to 1:2.2.
9. The method of claim 1 wherein the metal halide is zinc chloride.
10. The method of claim 1 wherein the promoter is chlorosulphonic acid, a C 1 -C 12 alkyl sulphonic acid, a C 6 -C 12 aryl sulphonic acid, a C 1 -C 12 alkyl C 6 -C 12 aryl sulphonic acid, a halogenated C 1 -C 12 alkyl sulphonic acid, a halogenated C 6 C 12 aryl sulphonic acid, a halogenated C 1 -C 12 alkyl C 6 -C 12 aryl sulphonic acid, trichloroacetic acid, triflic acid, boron trifluoride, or a combination comprising at least one of the foregoing promoters.
11. The method of claim 10 wherein the promoter is chlorosulphonic acid.
12. The method of claim 1 wherein the reaction is conducted with stirring and wherein, as measured after reaction for 20 hours, stirring is at a torque that is less than 3.0 Nm.
13. The method of claim 1 wherein, following reaction, the reaction is quenched with an organic solvent to form a solid phase comprising the phenolphthalein compound and a liquid phase comprising the ionic liquid catalyst composition, the solid phase is separated from a liquid phase, and the ionic liquid catalyst composition is recovered from the liquid phase.
14. The method of claim 13 , further comprising reusing the recovered ionic liquid catalyst composition for at least one additional reaction cycle to form the phenolphthalein compound.
15. The method of claim 14 wherein unused ionic liquid catalyst composition is mixed with the recovered used ionic liquid catalyst composition in the at least one additional reaction cycle.
16. The method of claim 13 , wherein the phenolphthalein compound in the separated solid phase is mixed with an aqueous solvent, filtered, and washed with aqueous solvent to obtain a purified phenolphthalein compound in a yield of greater than or equal to 70 mol %, based on the moles of phthalic anhydride compound.
17. The method of claim 1 further comprising converting the phenolphthalein compound to 2-phenyl-3,3-bis(4-hydroxyphenyl)phthalimidine.
18. The method of claim 1 further comprising polymerizing the 2-phenyl-3,3-bis (4-hydroxyphenyl)phthalimidine to form a polycarbonate.
19. A method for producing a phenolphthalein compound, comprising:
reacting a phenolic compound of the formula:
wherein R a is a hydrogen or a C 1 -C 12 hydrocarbyl group, with a phthalic anhydride compound of the formula:
wherein R b is a hydrogen, a C 1 -C 12 hydrocarbyl group, or a halogen, in the presence of an ionic liquid catalyst composition and a promoter to form a reaction mixture comprising a phenolphthalein compound of the formula:
wherein each R a is independently a hydrogen or a C 1 -C 12 hydrocarbyl group, and R b is a hydrogen, a C 1 -C 12 hydrocarbyl group, or a halogen;
wherein the ionic liquid catalyst composition comprises a combination of an ionic liquid and a metal halide wherein the metal is selected from the group consisting of zinc, iron, and a combination thereof.
20. A method for producing a phenolphthalein compound comprising:
reacting a phenolic compound of the formula:
wherein R a is a hydrogen or a C 1 -C 12 hydrocarbyl group, with a phthalic anhydride compound of the formula:
wherein R b is a hydrogen, a C 1 -C 12 hydrocarbyl group, or a halogen, at a temperature of 100° C. to 175° C. in the presence of an ionic liquid catalyst composition and promoter to form a reaction mixture comprising a phenolphthalein compound of the formula:
wherein each R a is the same and is a hydrogen or a C 1 -C 12 hydrocarbyl group, and R b is a hydrogen, a C 1 -C 12 hydrocarbyl group, or a halogen;
wherein the ionic liquid catalyst composition is present in an amount of 25 to 75 wt. % based on the weight of the reaction mixture and comprises a combination of an ammonium salt that is a liquid at 25° C., and zinc chloride; and
wherein the reaction is carried out with stirring at a torque that, measured after 20 hours of reaction, is less than 3.0 Nm; and
wherein the phenolphthalein compound is obtained in a yield of greater than or equal to 70 mol %, based on the moles of phthalic anhydride compound.
21. The method of claim 20 wherein the phenolphthalein compound obtained has a purity of greater than or equal to 80 weight percent, based on the weight of the precipitate.