Title of Invention

PROCESS FOR THE PREPARATION OF 2,3,5- TRIMETHYLHYDROQUINONE DIACYLATES

Abstract 2,3,5-Trimethyl-1,4-hydroquinone diacylates are obtained by reacting 3,5,5-trimethyl-1,4-benzoquinone with an acylating agent in the presence of methane trisulfonic acid as a catalyst.
Full Text Process for the preparation of 2,3,5-trimethylhydroquinone diacylates
The present invention is concerned with a process for the preparation of 2,3,5-trimethylhydroquinone diacylates by reacting 3,5,5-trimethyl-l,4-benzoquinone (ketoisophorone) with an acylating agent in the presence of methanetrisulfonic acid. 2,3,5-Trimethylhydroquinone diacylates are useful as reactants for the preparation of 2,3,5-trimethylhydroquinone, itself a known valuable reactant for the preparation of (all-rac)-α-tocopherol.
2,3,5-Trimethylhydroquinone diacylates are known to be producible by reacting ketoisophorone with an acylating agent in the presence of a strongly acidic catalyst. Many such catalysts have been proposed in the past for this purpose, in particular protonic acids, e.g. such inorganic acids as sulphuric acid; such organic acids as p-toluenesulphonic acid; strongly acidic ion exchange resins; and such Lewis acids as zinc chloride, boron trifluoride, antimony pentafluoride and titanium tetrachloride: see inter alia German Offenlegungsschrift 2149159 and European Patent Publications EP 0916642 Al and EP 1028103 Al; as well as NH-acidic or CH-acidic catalysts, see PCT Publication WO 03/051812.
It has now been found that by the use of small amounts of methanetrisulfonic acid, the conversion of ketoisophorone to 2,3,5-trimethylhydroquinone diacylates can be accomplished in high yield and without the need to use additional solvents. The use of methanetrisulfonic acid as the catalyst provides, all in all, advantages over catalysts used so far in this reaction in terms of stability of the catalyst, high yield, selectivity, and costs.
Thus, the presence invention relates to a process for the preparation of 2,3,5-trimethyl-l,4-hydroquinone diacylates by reacting 3,5,5-trimethyl-l,4-benzoquinone with an acylating agent in the presence of methane trisulfonic acid.
The acylating agent used in the process of the present invention may be any acylating agent that is conventionally used in the conversion of ketoisophorone to 2,3,5-trimethylhydroquinone acylates, particularly acid anhydrides, acyl halides, and enol esters. Examples of acid anhydrides are straight or branched chain alkanoic acid anhydrides such as acetic, propionic and butyric anhydride. Examples of acyl halides are straight or branched chain alkanoyl chlorides such as acetyl, propionyl and butyryl chloride. Finally, examples of enol esters are isopropenyl acetate and butyrate. The preferred acylating agent is acetic anhydride or acetyl chloride, especially acetic anhydride.
The process of the present invention can be carried out in the absence of a solvent. While the ratio of acylating agent to ketoisophorone is not narrowly critical the molar ratio of acylating agent to ketoisophorone is suitably from about 1: 1 to about 10:1, preferably from about 5 :1 to about 3 :1, and is most preferably about 3 :1.
The amount of catalyst, methane trisulfonic acid, is suitably about 0.01 to about 2.0 mole%, preferably about 0.075 to about 1.5 mole%, and most preferably about 0.1 to about 1.0 mole%, based on the amount of ketoisophorone.
The process is conveniently carried out at temperatures from about 0 °C to about 140 °C, preferably from about 20 °C to about 90 °C, especially 20 °C to 70 °C.
The process according to the present invention may be carried out batchwise or in continuous mode. Moreover, the process is conveniently carried out under an inert gas atmosphere, preferably under gaseous nitrogen or argon.
The progress of the reaction is suitably monitored by gas chromatography and mass spectrometry of samples taken from the reaction mixture at various time intervals during the reaction.
The produced 2,3,5-trimethylhydroquinone diacylate can be isolated after distilling off the remaining acylating agent and the secondary product formed in the acylation, e.g. acetic acid when acetic anhydride is used as the acylating agent, by extraction of the crude product mixture with a suitable organic solvent, e.g. toluene. For instance, in effecting this procedure using acetic anhydride as the acylating agent 2,3,5-trimethylhydroquinone diacetate was obtained as colourless crystals after evaporating off the toluene used as the extracting solvent. Another isolation procedure is the crystallization of the 2,3,5-trimethylhydroquinone diacylate from the mixture at the termination of the reaction by cooling, and, optionally, adding water, to the mixture to promote the crystallization.
The catalyst can be recovered by extraction with water or acid-water and concentration of the extract. Alternatively, the catalyst can be recovered by adding a
biphasic solvent system, e. g. a carbonate (particularly ethylene carbonate or propylene carbonate) and an aliphatic hydrocarbon (particularly heptane or octane), and isolating it from the polar (carbonate) phase
The 2,3,5-trimethylhydroquinone diacylate obtained by the process of the present invention can be converted into 2,3,5-trimethylhydroquinone by transesterification, i.e. by treatment with an alcohol, e.g. an aliphatic alcohol such as isopropanol or n-butanol. Depending on the amounts of alcohol and catalyst and on the temperature in the reaction mixture, the transesterification yields the unesterified 2,3,5-trimethylhydroquinone and the ester formed as the further product. 2,3,5-Trimethylhydroquinone can be converted into (all-rac)-a-tocopherol by known procedures by reaction with isophytol, preferably In a biphasic solvent system, e.g. in a solvent system comprising a polar solvent such as ethylene or propylene carbonate, and an non-polar solvent, particularly an aliphatic hydrocarbon such as heptane, see, e.g. international application PCT/EP03/01556.
The invention is illustrated further by the following Examples.
Example 1
A 50-ml four-necked flat-bottomed flask equipped with a thermometer, a glass-tube (0 5 mm) for Ar-purge, a reflux condenser and a magnetic stirring bar was charged with methanetrisulfonic acid (see Table 1 below) and 10.324 g (66 mmol) of ketoisophorone. Within 2 min, acetic anhydride was added dropwise (see Table 1 below) under rapid stirring. During addition, the mixture turned dark yellow to finally dark brown and the internal temperature increased. After cooling to the desired reaction temperature that temperature was maintained by means of an oil bath. Samples were withdrawn and submitted to qualitative GC-analysis. After the reaction time (see Table 1 below), the reaction mixture was cooled to room temperature and the catalyst was deactivated by addition of 3.7 g (70 mmol) anhydrous sodium carbonate. The reaction mixture was concentrated by 40°C/10mbar thereby distilling off acetic acid and unreacted anhydride. The crude product was analyzed by GC using squalane as internal standard. The results and reactions conditions are given in Table 1 below (Table Removed)
(
The values given are averages from several measurements (two or three) and two experiments.
AcaO : acetic anhydride; TMHQ-DA: 2,3,5-trimethyl-l,4-hydroquinone diacetate [yield]
Example 2
Using a 230 mi-flask the procedure of Example 1 was repeated with changing ratios of ketoisophorone and acetic anhydride. The reaction conditions and results are given in Table 2 below:

(Table Removed)The values given are averages from several measurements (two or three) and two experiments. S: Selectivity.
Example 3
In analogy to the procedure of Example 1, the reaction conditions were optimized using a statistical model (STAVEX). 20.32 g (200 mmol) of acetic anhydride were added within 10 min. to 10.324 g (66 mmol) of ketoisophorone. The results are tabulated in Table 3 below:

(Table Removed)Example 4
Based on the results of Example 3, experiments under optimized conditions were carried
out. The results are summarized in Table 4
Table 4
(Table Removed)




We claim:
1. A process for the preparation of 2,3,5-trimethyl-1,4-hydroquinone diacylates by reacting ketoisophorone with an acylating agent in the presence of methane trisulfonic acid.
2. The process as claimed in claim 1, wherein the reaction is carried out in the presence of about 0.01 mol% to about 2 mol% of methane trisulfonic acid, based on ketoisophorone.
3. The process as claimed in claim 2, wherein the reaction is carried out in the presence of about 0.1 mol% to about 1 mo1% of methane trisulfonic acid, based on ketoisophorone.
4. The process as claimed in any one of claims 1 to 3, wherein the molar ratio of acylating agent to ketoisophorone is about 10 to 1, preferably about 3 to 1.
5. The process as claimed in any one of claims 1 to 4, wherein the acylating agent is acetic anhydride.
6. The process as claimed in any one of claims 1 to 5, wherein the reaction is carried out at about 0 °C to about 140 °C, preferably at about 20 °C to about 70 °C.

Documents:

2386-delnp-2006-abstract.pdf

2386-DELNP-2006-Claims-(24-06-2011).pdf

2386-delnp-2006-claims.pdf

2386-DELNP-2006-Correspondence Others-(24-06-2011).pdf

2386-delnp-2006-correspondence-others-1.pdf

2386-delnp-2006-correspondence-others.pdf

2386-delnp-2006-description (complete).pdf

2386-delnp-2006-form-1.pdf

2386-delnp-2006-form-18.pdf

2386-delnp-2006-form-2.pdf

2386-delnp-2006-form-3.pdf

2386-delnp-2006-form-5.pdf

2386-delnp-2006-gpa.pdf

2386-delnp-2006-pct-210.pdf

2386-delnp-2006-pct-409.pdf

2386-DELNP-2006-Petition-137-(24-06-2011).pdf


Patent Number 249379
Indian Patent Application Number 2386/DELNP/2006
PG Journal Number 42/2011
Publication Date 21-Oct-2011
Grant Date 18-Oct-2011
Date of Filing 28-Apr-2006
Name of Patentee DSM IP ASSETS B. V.
Applicant Address HET OVERLOON 1, NL-6411 TE HEERLEN, THE NETHERLANDS.
Inventors:
# Inventor's Name Inventor's Address
1 BONRATH, WERNER 29 LUCKENBACH WEG, 79115 FREIBURG, GERMANY.
2 PACE, FRANCESCO SALZBODENSTRASSE 6, CH - 4310 RHEINFEIDEN, SWITZERLAND.
3 AQUINO, FABRICE 34A RUE DE LEIMBACH, F-68950 REININGUE, FRANCE.
PCT International Classification Number C07C 67/08
PCT International Application Number PCT/EP2004/012058
PCT International Filing date 2004-10-26
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 03025513.7 2003-11-07 EUROPEAN UNION