Process for preparing heterocyclic (R)- and (S)-cyanohydrins

US7052885B2 · kind B2 · utility

Assignee

• DSM Fine Chemicals Austria NFG GmbH & Co KG · AT

Inventors

• Peter Poechlauer · Linz, AT
• Wolfgang Skranc · Wien, AT
• Herbert Mayrhofer · Linz, AT
• Irma Wirth · Ansfelden, AT
• Rudolf Neuhofer · Mittertreffling, AT
• Herfried Griengl · Graz, AT
• Martin Fechter · Graz, AT

Key dates

• Filing date: Dec 23, 2002
• Grant date: May 30, 2006
• Expiry date: Nov 19, 2023

Classification

• Technology area (CPC C): Chemistry; Metallurgy
• CPC primary: C12P17/04
• WIPO field: Biotechnology
• WIPO sector: Chemistry

Abstract

A process for preparing enantiomer-enriched heterocyclic (R)- and (S)-cyanohydrins of the formula (I),where R1, R2, R3, R4 independently of one another are H, an unsubstituted or substituted C1–C24-alkyl, alkenyl or alkynyl radical, where one or more carbon atoms in the chain can be replaced by an oxygen atom, a nitrogen atom, a sulfur atom, an SO or an SO2 group, an unsubstituted or substituted aryl or heteroaryl radical or heterocyclic radical or halogen, hydroxyl, NR5R6, acetyl, oxo, C1–C6-carbalkoxy, C1–C6-carbalkoxyamino, COOR7, cyano, amide, benzoylamino or NO2,R5 and R6 are H, C1–C6-alkyl radical, phenyl radical, benzyl radical or COOR7, or together form a C2–C8-alkylene or heteroalkylene radical,R7 is H or C1–C6-alkyl,n is 0, 1, 2 or 3,X, Y and Z can be an unsubstituted or substituted carbon atom or a radical selected from the group consisting of N, O, S or NR5R6, where R5 and R6 are as defined above, SO or SO2, and at least one of the radicals X, Y and Z is not a carbon atom, where the compounds of the formula (I) can have one or more double bonds in the ring, with the proviso that in a 5-membered ring the double bond is not conjugated with the —C(OH)CN-group, and/or can b…