Process for the epoxidation of a tetrasubstituted alkene

16:

• A process for the epoxidation of a tetrasubstituted alkene to the corresponding epoxide comprising reacting the tetrasubstituted alkene with performic acid prepared in situ from formic acid and hydrogen peroxide in the presence of at least one buffering agent
• wherein the tetrasubstituted alkene is terpinolene of the formula (Ia)
• and the corresponding epoxide is terpinolene epoxide of formula (IIa)

17:

• The process according to claim 16 wherein the buffering agent is selected from salts of inorganic acids, salts of organic acids and any combination thereof.

18:

• The process according to claim 16 wherein the buffering agent is a salt selected from phosphates, formates, acetates, carbonates, citrates, sulfates and any combination thereof.

19:

• The process according to claim 16 wherein the buffering agent is selected from alkali metal and alkaline earth metal phosphates, alkali metal and alkaline earth metal formates and any combination thereof.

20:

• The process according to claim 16 wherein the buffering agent is selected from alkali metal phosphates.

21:

• The process according to claim 16 wherein the buffering agent is selected from di-(alkali metal) hydrogen phosphates.

22:

• The process according to claim 16 wherein the reaction is carried out in the presence of at least one inert organic solvent.

23:

• The process according to claim 22 wherein the inert organic solvent is selected from non-halogenated aliphatic hydrocarbons, non-halogenated cycloaliphatic hydrocarbons, non-halogenated aromatic hydrocarbons, halogenated aliphatic hydrocarbons, halogenated aromatic hydrocarbons, amides, ethers, esters, ketones, nitriles and any combination thereof.

24:

• The process according to claim 22 wherein the inert organic solvent is selected from non-halogenated inert organic solvents.

25:

• The process according to claim 16 wherein the temperature is from 0 to 70° C.

26:

• The process according to claim 16 wherein the terpinolene epoxide of formula (IIa) is further converted via limonene-4-ol to terpinene-4-ol.

27:

• The process according to claim 16, wherein the terpinolene epoxide of formula (IIa), limonene-4-ol or terpinene-4-ol is further converted into (+)-2-exo-(2-Methylbenzyloxy)-1-methyl-4-isopropyl-7-oxabicyclo[2.2.1]heptane, any of its individual enantiomers or any non-racemic mixture thereof.

28:

• Use of an oxidizing agent comprising hydrogen peroxide and formic acid for the selective in-situ epoxidation of the exocyclic double bond in terpinolene of the formula (Ia)