Production of methyl-vinyl ketone from levulinic acid
Abstract
A method for converting levulinic acid to methyl vinyl ketone is described. The method includes the steps of reacting an aqueous solution of levulinic acid, over an acid catalyst, at a temperature of from room temperature to about 1100 K. Methyl vinyl ketone is thereby formed.
- Inventors:
-
- Verona, WI
- Madison, WI
- Issue Date:
- Research Org.:
- Univ. of Delaware, Newark, DE (United States)
- Sponsoring Org.:
- USDOE
- OSTI Identifier:
- 1019095
- Patent Number(s):
- 7960592
- Application Number:
- US Patent Application 12/685,887
- Assignee:
- Wisconsin Alumni Research Foundation (Madison, WI)
- Patent Classifications (CPCs):
-
C - CHEMISTRY C07 - ORGANIC CHEMISTRY C07C - ACYCLIC OR CARBOCYCLIC COMPOUNDS
- DOE Contract Number:
- FG02-03ER15468
- Resource Type:
- Patent
- Country of Publication:
- United States
- Language:
- English
- Subject:
- 37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
Citation Formats
Dumesic, James A., and West, Ryan M. Production of methyl-vinyl ketone from levulinic acid. United States: N. p., 2011.
Web.
Dumesic, James A., & West, Ryan M. Production of methyl-vinyl ketone from levulinic acid. United States.
Dumesic, James A., and West, Ryan M. Tue .
"Production of methyl-vinyl ketone from levulinic acid". United States. https://www.osti.gov/servlets/purl/1019095.
@article{osti_1019095,
title = {Production of methyl-vinyl ketone from levulinic acid},
author = {Dumesic, James A. and West, Ryan M.},
abstractNote = {A method for converting levulinic acid to methyl vinyl ketone is described. The method includes the steps of reacting an aqueous solution of levulinic acid, over an acid catalyst, at a temperature of from room temperature to about 1100 K. Methyl vinyl ketone is thereby formed.},
doi = {},
journal = {},
number = ,
volume = ,
place = {United States},
year = {2011},
month = {6}
}
Works referenced in this record:
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Levulinic acid synthesis via regiospecific carbonylation of methyl vinyl ketone ob of its reaction products with hydrochloric ach) or an alkanol or of a mixture of acetone with a formaldehyde precursor catalyzed by a highly active Pd-HCl system
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