Acetone → Butyric Acid
Reaction equation
CCC.C([OH:7])(C)C.CC(C)=O.[CH2:12]([OH:16])[CH2:13][CH2:14][CH3:15]>C(C(C)=O)C.CC(O)CC>[CH3:12][CH2:13][CH2:14][CH3:15].[C:12]([OH:7])(=[O:16])[CH2:13][CH2:14][CH3:15]Participants
Reactant 4
Product 2
Reagents, catalysts & solvents 2
Procedure
Oxidation of alkanes can give a variety of oxygenated products, including alcohols (see, e.g., U.S. Pat. Nos. 4,918,238, 4,978,799, 5,235,111, 5,345,010, 5,354,857, 5,409,876, and 5,663,328), aldehydes (see, e.g., J. Catal., 202(2) (2001) 308; Appl. Catal., A 217(1-2) (2001) 111; U.S. Pat. No. 4,859,798), ketones (e.g., Appl. Catal., A 217(1-2) (2001) 111; EP 0126488; U.S. Pat. Nos. 4,038,322, 5,235,111, and 5,409,876), carboxylic acids and anhydrides (see, e.g., U.S. Pat. Nos. 5,543,532, 5,663,328, 6,646,158, 6,919,295, and 6,914,029). Oxidation of propylene may produce isopropanol, acetone, propionaldehyde, acrolein, acrylic acid, propionic acid, and the like, and mixtures thereof. Under appropriate reaction conditions, oxidation of propane may give isopropanol, acetone, or a mixture of them. Oxidation of n-butane may produce 1-butanol, 2-butanol, methyl ethyl ketone, n-butylaldehyde, n-butyric acid, maleic acid, maleic anhydride, and the like, and mixtures thereof.
Workup
- additiona mixture of them
Sources & evidence
- ORD record
- ord-0b316672d4d1441f81de7f34ceb73ebc
- Source dataset
- uspto-grants-2008_04
- Patent number
- US07365217B2
Reaction notes
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