6533b7d3fe1ef96bd1261240

RESEARCH PRODUCT

Efficient Resolution of Menthylamine with Inexpensive (R,R)-Tartaric Acid by Dielectrically Controlled Resolution (DCR)

Siegfried R. WaldvogelMagdalena SchmittDieter Schollmeyer

subject

Solvent systemChemistryOrganic ChemistryDiastereomerChiral resolutionchemistry.chemical_compoundTartaric acidOrganic chemistryAmine gas treatingMethanolPhysical and Theoretical ChemistrySolvent effectsEnantiomerNuclear chemistry

description

A practical procedure for the resolution of menthylamine 2 with (R,R)-tartaric acid [(R,R)-3] as resolving agent is presented. Variation of the solvent system allows both enantiomers of 2 to be selectively crystallized. Performing the resolution in methanol containing 6 % water leads to (–)-2·(R,R)-3·MeOH. The other, less-soluble diastereomeric salt is obtained by applying a solvent system consisting of methanol with 19 % water with a yield of 14 %. Subsequent basic workup with aqueous sodium hydroxide gave the free menthylamine compounds. Further workup of the mother liquors and an additional recrystallization step allowed the (–)-2·(R,R)-3·MeOH salt to be obtained in an overall yield of 22 %; the other salt (+)-2·(R,R)-3·MeOH·H2O was obtained in 23 % yield. This is another important example of the dielectrically controlled resolution of an interesting amine by using inexpensive (R,R)-tartaric acid as resolving agent.

https://doi.org/10.1002/ejoc.201301566