OXIDATION OF SANTALENE TO SANTALOL

Abstract

The invention relates to a process for the oxidation of santalene to santalol. The starting material is in particular a mixture comprising alpha-santalene, beta-santalene, epi-beta-santalene, trans-alpha-bergamotene and beta-bisabolene. The oxidation of the santalenes occurs via an intermediate chloro-santalene compound. Substitution of the chloro-substituent by acetate yielded the mixture of the corresponding santalyl actates, which were hydrolyzed to yield the corresponding mixture of santalols.

Claims

1-16 (canceled)

17. Process for the synthesis of a compound of Formula (I) ##STR00021## wherein R=a, b, c, d or e; ##STR00022## comprising the chlorination of a starting compound of Formula (II) ##STR00023## to an intermediate of Formula (III) ##STR00024## the conversion of the intermediate of Formula (III) to the compound of Formula (I); wherein the chlorination comprises combining the starting compound of Formula (II) with an acid and an aqueous NaOCl solution.

18. Process according to claim 17, wherein the acid is a carboxylic acid.

19. Process according to claim 18, wherein the carboxylic acid is selected from the group of formic acid, acetic acid, chloroacetic acid, dichloroacetic acid, trichloroacetic acid, propionic acid, 2-chloropropionic acid, 3-chloropropionic acid, trifluoroacetic acid, butyric acid, valeric acid, caproic acid, heptanoic acid, caprylic acid and benzoic acid.

20. Process according to claim 17, wherein the acid is present in an amount in the range of 1.05-3.0 acid equivalents relative to the NaClO in particular in the range of 1.1-2.0 acid equivalents, more in particular in the range of 1.2-1.5 acid equivalents.

21. Process according to claim 17, wherein the NaOCl is present in an amount in the range of 1.1-1.9 molar equivalents relative to the starting compound of Formula (II), in particular in the range of 1.3-1.7 molar equivalents.

22. Process according to claim 17, wherein the acid is present in an amount in the range of 1.2-1.5 acid equivalents relative to the NaOCl while the NaOCl is present in an amount in the range of 1.25-1.75 molar equivalents relative to the starting compound of Formula (II).

23. Process according to claim 17, wherein the chlorination is performed in the presence of an organic solvent, in particular a solvent selected from the group toluene, dichloromethane and methylcyclohexane.

24. Process according to claim 17, wherein the conversion of the intermediate of Formula (III) to the compound of Formula (I) is performed by reacting the intermediate of Formula (III) with a carboxylate R′—COO.sup.− to form the corresponding carboxylate ester of Formula (IV), wherein R′ comprises an alkyl group of 1-7 carbon atoms; thereafter ##STR00025## hydrolyzing the ester of Formula (IV) to the corresponding compound of Formula (I).

25. Process according to claim 24, wherein the carboxylate is acetate, formate or propionate.

26. Process according to claim 17, wherein the chlorination is performed on a mixture of compounds of Formula (II) to yield a mixture of the corresponding intermediates of Formula (III); and the mixture of intermediates of Formula (III) is converted to a mixture of the corresponding compounds of Formula (I).

27. Process according to claim 26, wherein the mixture of compounds of Formula (II) comprises the compounds of Formula (IIa), Formula (IIb), Formula (IIc), Formula (IId) and Formula (IIe).

28. Process according to claim 27, wherein the chlorination of the mixture comprises the conversion of the starting compounds of Formula (IIa), Formula (IIb), Formula (IIc) and Formula (IIe) to the intermediates of Formula (IIIa), Formula (IIIb), Formula (IIIc) and Formula (IIIe); and the introduction of two or three chloro-substituents on the starting compound of Formula (IId) to yield a di-chlorinated and/or a tri-chlorinated analogue of the intermediate of Formula (IIId); and wherein the di-chlorinated and/or tri-chlorinated analogue is/are removed from the mixture prior to or during the conversion of the intermediates of Formula (IIIa), Formula (IIIb), Formula (IIIc) and Formula (IIIe) to the corresponding santalol sesquiterpenoids of Formula (Ia), Formula (Ib), Formula (Ic) and Formula (Ie).

29. Process according to claim 28, wherein the NaOCl is present in the chlorination reaction in an amount in the range of 2.1-3.5 molar equivalents relative to the starting compound of Formula (IId), preferably in the range of 2.2-3.2 molar equivalents.

30. Process according to claim 28 wherein the compound of Formula (I) is produced in isomers (Z and E) in a ratio of 55:45, preferably 60:40, more preferably 65:35 or higher.

31. Compound of Formula (III) ##STR00026## wherein R=d or e; ##STR00027##

32. A composition comprising bergamotol, preferably trans-alpha-bergamotol, Z santalol and E santalol, wherein bergamotol, preferably trans-alpha-bergamotol, is not more than 10% (w/w) and Z santalol is in excess of E santalol.

Description

EXAMPLES

1. Chlorination of Santalene Sesquiterpenes (II)

[0078] In a 250 mL three-necked round bottom flask equipped with a magnetic stirrer, a thermometer and a dropping funnel, the santalene mix (10.0 g, obtained via the procedures as described in WO2018/160066), toluene (75 mL) and AcOH (6.0 mL) were added. NaOCl (14% Cl.sub.2 solution) (33.75 and 34.50 mL) was put in the dropping funnel and added very slowly to the reaction mixture over a period of 2 h. An aliquot of the reaction was extracted and analyzed by GC. Afterwards, NaOCl (14% Cl.sub.2 solution)(1 mL portions) was added in 30 min intervals until the starting santalene mixture (II) was fully converted to products. After completion of the reaction, NaHCO.sub.3 solution was added to the reaction mixture and the organic phase was extracted. The organic phase was washed twice with NaCl solution, dried and the solvent evaporated in vacuo furnishing a yellow oil (11.98 g). The residue was analyzed by GC. About 80% of trans-alpha-berga-motene was converted to derivates and these unwanted bergamotene derivates are easily removable by distillation.

2. Substitution of the Chloro-Group of Chloro-Santalenes (III)

[0079] A 100 mL round bottom flask equipped with a magnetic stirrer was charged with the KOAc (7.46 g), Kl (800 mg) and the chloro-santalene mix (5.0 g) obtained under Example 1 were added. DMA (30 mL) or Toluene/TBAB (30 mL/250 mg) were added as solvent. The reaction was placed in an oil bath and stirred at 110° C. in a 2h reaction (DMA) or an overnight reaction (toluene/TBAB). The reaction progress was monitored by GC. After completion of the reaction, the reaction mixture was cooled down to room temperature and aqueous NaHCO.sub.3 solution and n-pentane were added. The reaction mixture was transferred to a dropping funnel and the organic phase was extracted and washed with brine (or several times with LiCl solution in the case of DMA). The organic phase was dried over sodium sulfate, filtered and the solvent evacuated in vacuo to yield a light yellow oil. The residue was analyzed by GC and NMR.

3. Hydrolysis of the Santalyl Acetate Esters (IV)

[0080] A 100 mL round bottom flask equipped with a magnetic stirrer was charged with the santalyl acetates mixture (5.0 g) obtained under Example 2, KOH (5.0 g), H.sub.2O (6.8 mL) and MeOH (34 mL). The reaction mixture was heated to 60° C. for 10 min and stirred at room temperature for an additional 30 min. After completion of the reaction, water (ca. 60 mL) and n-pentane/Ac—OEt (4/1; 60/15 mL) were added to the reaction mixture. The organic phase was extracted and washed with brine. The organic phase was then dried over sodium sulfate and filtered. The solvent was removed in vacuo, furnishing a light yellow oil (4.0 g) which was analyzed by GC. The santalol sesquiterpenoids of Formula (I) were isolated as a mixture after distillation of this oil.

[0081] The conversion of santalene to santalol was above 90% and santalol was formed as two conformational-isomers (Z and E) in a 65:35 ratio. It was also found that trans-alpha-bergamotene resulted in trans-alpha-bergamotol present at much lower levels as the level of the initial trans-alpha-bergamotene and compared to levels when no over-chlorination was applied.

[0082] When in experiment 2 potassium formate replaced potassium acetate even better results were achieved.

LITERATURE CITED

[0083] Nussbaumer, C., Fráter, G. and Kraft, P. (1999), (±)-1-[(1R*,2R*,8aS*)-1,2,3,5,6,7,8,8a-Octahydro-1,2,8,8-tetramethylnaphthalen-2-yl]ethan-1-one: Isolation and Stereoselective Synthesis of a Powerful Minor Constituent of the Perfumery Synthetic Iso E Super®. HCA, 82: 1016-1024. doi:10.1002/(SIC1)1522-2675(19990707)82:7<1016::AID-HLCA1016>3.0.CO;2-Y