Claims
- 1. Method of making methyl isopropenyl ketone comprising reacting methyl ethyl ketone and paraformaldehyde in the presence of a secondary amine hydrohalide and a catalyst selected from (a) a carboxylic acid having up to about 15 carbon atoms and (b) a solid non-soluble oxide of an element of Group IB, IIIA, IVA, VA, VB, VIB and VIII of the periodic table.
- 2. Method of making methyl isopropenyl ketone comprising reacting methyl ethyl ketone with paraformaldehyde in the presence of an amine catalyst of the formula R.sup.1 R.sup.2 NH, a halogen acid, and a solid catalyst selected from the group consisting of non-soluble oxides of elements of Groups IB, IIIA, IVA, IVB, VA, VB, VIB and VIII of the periodic table, where R.sup.1 and R.sup.2 are independently selected alkyl or aryl groups having up to about 20 carbon atoms or forming hetero groups in combination having up to about 20 carbon atoms.
- 3. Method of claim 2 wherein the ratio of methyl ethyl ketone to paraformaldehyde is about 10:1 to about 1:10.
- 4. Method of claim 2 wherein the ratio of methyl ethyl ketone to paraformaldehyde is about 5:1 to about 1:1.
- 5. Method of claim 2 wherein the temperature is maintained in the range of about 50.degree. C. to about 250.degree. C.
- 6. Method of claim 2 wherein the pressure is maintained at about 700-1400 kilopascals.
- 7. Method of claim 2 wherein the amine catalyst is present in an amount from about 0.01 equivalent to about 0.1 equivalent with respect to the methyl ethyl ketone reactant.
- 8. Method of claim 2 wherein the halogen acid is present in the form of a salt of the amine catalyst.
- 9. Method of claim 2 wherein the solid catalyst is present in an amount from about 0.0025 to about 0.1 equivalent with respect to the methyl ethyl ketone reactant.
- 10. Method of claim 2 wherein the solid catalyst is present in an amount from about 0.01 to about 0.025 equivalent with respect to the methyl ethyl ketone reactant.
- 11. Method of claim 2 wherein the solid catalyst is niobium oxide.
- 12. Method of making methyl isopropenyl ketone and ethyl vinyl ketone comprising reacting paraformaldehyde with methyl ethyl ketone in the presence of a catalyst which is a halogen acid salt of an amine of the formula R.sup.1 R.sup.2 NH, where R.sup.1 and R.sup.2 are independently selected alkyl or aryl groups having up to about 20 carbon atoms or forming hetero groups in combination having up to about 20 carbon atoms, and a solid catalyst selected from the group consisting of non-soluble oxides of elements of Groups IB, IIIA, IVA, IVB, VA, VB, VIB and VIII of the periodic table.
- 13. Method of claim 12 wherein the solid catalyst is present in a bed.
- 14. Method of claim 12 wherein the solid catalyst is niobium oxide.
- 15. Method of making a methyl isopropenyl ketone and ethyl vinyl ketone comprising reacting methyl ethyl ketone with paraformaldehyde in the presence of an amine catalyst of the formula R.sup.1 R.sup.2 NH, a halogen acid, and a small amount of a carboxylic acid having up to about 15 carbon atoms, where R.sup.1 and R.sup.2 are independently selected alkyl or aryl groups having up to about 20 carbon atoms.
- 16. Method of claim 15 wherein the ratio of methyl ethyl ketone to paraformaldehyde is about 10:1 about 1:10.
- 17. Method of claim 15 wherein the ratio of methyl ethyl ketone to paraformaldehyde is about 5:1 to about 1:1.
- 18. Method of claim 15 wherein the temperature is maintained in the range of about 50.degree. C. to about 250.degree..
- 19. Method of claim 15 wherein the pressure is maintained at about 700-1400 kilopascals.
- 20. Method of claim 15 wherein the amine catalyst is present in an amount from about 0.01 to about 0.1 equivalent with respect to the methyl ethyl ketone reactant.
- 21. Method claim 15 wherein the halogen acid is present in the form of a salt of the amine catalyst.
- 22. Method of claim 15 wherein the ratio of amine acid salt to carboxylic acid is about 0.5:1 to about 10:1.
- 23. Method of claim 15 wherein the carboxylic acid is propionic acid.
RELATED APPLICATIONS
This is a continuation-in-part of two prior applications of two of the inventors herein (J. Pugach and J. Salek), namely of application Ser. No. 367,902, filed June 19, 1989, now U.S. Pat. No. 4,945,184 entitled "Preparation of Unsaturated Ketones" and application Ser. No. 508,454, filed Apr. 13, 1990, now U.S. Pat. No. 5,004,839 entitled "Preparation of Unsaturated Ketones from Acetone and Paraformaldehyde (II)", the entire specifications and claims of which are incorporated herein by reference. Application Ser. No. 508,454 is in turn a continuation-in-part-of application Ser. No. 425,269, filed Oct. 23, 1989, now abandoned entitled "Preparation of Vinyl Ketones from Acetone and Paraformaldehyde (II)".
US Referenced Citations (10)
Non-Patent Literature Citations (1)
Entry |
Mironov et al., "Synthesis of alpha, beta-unsaturated Ketones", Yaroslavl' Technological Institute, translated from Zhurnal Prikladnoi Khimii, vol. 36, No. 3, pp. 654-662, Mar. 1963. |
Continuation in Parts (2)
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Number |
Date |
Country |
Parent |
367902 |
Jun 1989 |
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Parent |
425269 |
Oct 1989 |
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