Menthone

Menthone is a constituent of the essential oils of pennyroyal, peppermint, corn mint, pelargonium geraniums, and other plant species.^[1] In most essential oils, it is a minor component.^[5] Menthone was first synthesized by oxidation of menthol in 1881,^{[6][needs update][7]} before being found as a component in essential oils in 1891.^{[citation needed]} Of the isomers possible for this chemical structure (see below), the one termed l-menthone—formally, the (2S,5R)-trans-2-isopropyl-5-methylcyclohexanone (see infobox and below)—is the most abundant in nature.^[3]

Menthone is a liquid under standard conditions, and has a density of 0.895 g/cm³.^{[citation needed]} Under the same conditions,^{[verification needed]} the melting point is −6 °C, and its boiling point is 207 °C.^{[citation needed]}

Menthone interacts cognitively with other components in food, drink, and other consumables, to present with what is termed a minty flavor.^[2] Pure l-menthone has been described as having an intensely minty clean aroma;^{[according to whom?]} in contrast, d-isomenthone has a "green" note,^{[This quote needs a citation]} increasing levels of which are perceived to detract from the aroma quality of l-menthone.^{[8][verification needed]}

The structure of 2-isopropyl-5-methylcyclohexanone (menthones and isomenthones, see following) were established historically by establishing identity of natural and synthetic products after chemical synthesis of this structure from other chemical compounds of established structure; these inferential understandings have, in modern organic chemistry, been augmented by supporting mass spectrometric and spectroscopic evidence (e.g., from NMR spectroscopy and circular dichroism) to make the conclusions secure.^{[citation needed]}

The structure 2-isopropyl-5-methylcyclohexanone has two asymmetric carbon centers, one at each attachment point of the two alkyl group substituents, the isopropyl in the 2-position and the methyl in the 5-position of the cyclohexane framework.^{[9][better source needed]} The spatial arrangement of atoms—the absolute configuration—at these two points are designated by the descriptors R (Latin, rectus, right) or S (L., sinister, left) based on the Cahn–Ingold–Prelog priority rules.^[10] Hence, four unique stereoisomers are possible for this structure: (2S,5S), (2R,5S), (2S,5R) and (2R,5R).^{[9][better source needed]}

The (2S,5S) and (2R,5R) stereoisomers project the isopropyl and methyl groups from the same "side" of the cyclohexane ring, are the so-called cis isomers, and are termed isomenthone; the (2R,5S) and (2S,5R) stereoisomers project the two groups on the opposite side of the ring, are the so-called trans isomers, and are referred to as menthone.^{[9][better source needed]} Because the (2S,5R) isomer has an observed negative optical rotation, it is called l-menthone or (−)-menthone. It is the enantiomeric partner of the (2R,5S) isomer: (+)- or d-menthone.^{[9][better source needed][verification needed]}

Menthone and isomenthone interconvert easily, the equilibrium favoring menthone;^{[4][better source needed]} if menthone and isomenthone are equilibrated at room temperature, the isomenthone content will reach 29%.^{[dubious – discuss][8][verification needed]} Menthone can easily be converted to isomenthone and vice versa via a reversible epimerization reaction via an enol intermediate, which changes the direction of optical rotation, so that l-menthone becomes d-isomenthone, and d-menthone becomes l-isomenthone.^[11]

Menthone is obtained commercially by fractional crystallization of the oils pressed from peppermint and cornmint, sp. Mentha.^[4]

In the experimental laboratory, l-menthone may be prepared by oxidation of menthol with acidified dichromate.^{[12][needs update]} If the chromic acid oxidation is performed with stoichiometric oxidant in the presence of diethyl ether as co-solvent, a method introduced by H.C. Brown and colleagues in 1971, the epimerization of l-menthone to d-isomenthone is largely avoided.^[8]

Menthone was first described by Moriya in 1881.^[6][7] It was later synthesized by heating menthol with chromic acid, and its structure was later confirmed by synthesizing it from 2-isopropyl-5-methylpimelic acid.^[when?][9]

Menthone was one of the original substrates reported in the discovery of the still widely used synthetic organic chemistry transformation, the Baeyer-Villiger (B-V) oxidation,^[13] as reported by Adolf Von Baeyer and Victor Villiger in 1899; Baeyer and Villiger noted that menthone reacted with monopersulfuric acid to produce the corresponding oxacycloheptane (oxepane-type) lactone, with an oxygen atom inserted between the carbonyl carbon and the ring carbon attached to the isopropyl substituent.^[14]

In 1889, Ernst Beckmann discovered that dissolving menthone in concentrated sulfuric acid gave a new ketonic material which gave an equal but opposite optical rotation to the starting material.^{[15][non-primary source needed]} Beckmann's inferences from his results situated menthone as a crucial player in a great mechanistic discovery in organic chemistry.^{[clarification needed][citation needed]} Beckmann concluded that the change in structure underlying the observed opposite optical rotation was the result of an inversion of configuration at the asymmetric carbon atom next to the carbonyl group (which, at that time was believed to be the carbon atom attached to the methyl rather than the isopropyl group).^{[citation needed]} He postulated that this occurred through an intermediate enol—a tautomer of the ketone—such that the original absolute configuration of that carbon atom changed as its geometry went from terahedral to trigonal planar.^{[clarification needed][citation needed]} This report is an early example of an inference that an otherwise undetectable intermediate was involved in a reaction mechanism, one that could account for the observed structural outcome of the reaction.^{[according to whom?]}

• piperitone
• pulegone