Synthesis of alpha-amino acids
AssigneeThe United States of America as represented by the United States Department of Energy
InventorJefferson W. Davis, Jr.
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Abstract
A method for synthesizing alpha amino acids proceeding through novel intermediates of the formulas: R.sub.1 R.sub.2 C(OSOCl)CN, R.sub.1 R.sub.2 C(Cl)CN and [R.sub.1 R.sub.2 C(CN)O].sub.2 SO wherein R.sub.1 and R.sub.2 are each selected from hydrogen monovalent substituted and unsubstituted hydrocarbon radicals of 1 to 12 carbon atoms. The use of these intermediates allows the synthesis steps to be exothermic and results in an overall synthesis method which is faster than the synthesis methods of the prior art.
Claims5
An improved process for synthesizing an alpha-amino acid comprising:
- reacting a metal cyanide with an aldehyde or a ketone in the absence of water to form a corresponding cyanohydrin of the formula:
- R.sub.1 R.sub.2 C(OH)CN
- wherein R.sub.1 and R.sub.2 represent hydrogen, alkyl radicals of 1 to 10 carbon atoms, alkenyl radicals of 2 to 4 carbon atoms, aryl radicals of 6 to 12 carbon atoms, alkaryl radicals of 7-8 carbon atoms, aralkyl radicals of 7-8 carbon atoms, and p-hydroxyphenyl radicals,
- reacting said cyanohydrin with thionyl chloride to form a chlorosulfinyl nitrile of the formula:
- R.sub.1 R.sub.2 C(OSOCl)CN,
- reacting said chlorosulfinyl nitrile with ammonia to form an amino nitrile of the formula:
- R.sub.1 R.sub.2 C(NH.sub.2)CH;
- and,
- hydrolyzing said amino nitrile to the alpha-amino acid.
Dependencies are inferred from the claim text.