USPatent applicationPatented

Process for the preparation of 1,4-dialkyl-2,3-diol-1,4-butanedione

Granted 22 Jan 2008 · no office action yet

Current assignee: Firmenich SA · originally DSM-Firmenich

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Inventors: René Decorzant, Ferdinand Naef · Examiner: Sikarl A. Witherspoon · AU 1621 · TC 1600

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Abstract

The present invention relates to a process for the preparation of compounds of a 1,4-dialkyl-2,3-diol-1,4-butanedione by a catalytic aldol condensation between an alkyl glyoxal and an α-hydroxy ketone.

Description

7 parts
›CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of International application PCT/IB2005/053511 filed Oct. 27, 2005, the entire content of which is expressly incorporated herein by reference thereto.

›TECHNICAL FIELD

The present invention relates to the field of organic synthesis and more particularly to a new process for the preparation of 1,4-dione-2,3-diols as defined further below.

›BACKGROUND

The compounds of formula (I), as defined below, can be useful as starting material for the construction compounds having a more complex skeletons, such as 4-hydroxy-2,5-dimethyl-3(2H)-furanone (known as Furaneol®, Trademark of Firmenich SA).

Various processes for the preparation of compounds of formula (I) have been reported, for example Briggs et al, J. Chem. Soc. Perkin. Trans. I, 1985, 795 relates to a multistep synthesis of the 3,4-dihydroxyhexane-2,5-dione starting from the tartaric acid, or Bassignani et al, J. Org. Chem., 1978, 43, 4245 relates to the synthesis of the 3,4-dihydroxyhexane-2,5-dione by oxidizing the expensive 2,5-dimethylfuran with the toxic and expensive KClO 3 /OsO 4 system. Another reported method to synthesize compounds (I) is the reductive dimerisation of glyoxals promoted by various methods (for instance see EP 368211 or Büchi et al, J. Org. Chem., 1973, 38, 123).

The above-mentioned methods of preparation are in general quite long and expensive or imply the use of a large excess of heavy metal which implies problems of purification of the final product and of waste treatment.

To the best of our knowledge, in the prior art there is no report of an aldol condensation giving a direct access to compounds of formula (I).

›SUMMARY OF THE INVENTION

The present invention now relates to the field of organic synthesis and more particularly to a process for the preparation of compounds of formula (I) by the aldol condensation between an alkyl glyoxal (II) and an acetol derivative (III), said condensation being promoted a catalyst, according to Scheme (1):

wherein R 1 represents a linear or branched C 1 to C 5 alkyl group.

›DETAILED DESCRIPTION OF THE INVENTION

In order to overcome the problems aforementioned, and provide also an alternative process for the preparation of compounds (I), the present invention relates to a catalytic process aimed at the synthesis of compounds (I) in a single step and with good yields.

The process of the invention concerns more specifically the aldol condensation between an alkyl glyoxal (II) and an acetol derivative (III). Indeed, we have now surprisingly discovered that a specific type of catalyst is able to promote the invention reaction.

Therefore, the process of the invention concerns the preparation of a compound of formula

wherein R 1 represents a linear or branched C 1 to C 5 alkyl radical,

said process being characterized in that it comprises the aldol condensation, in a water-containing reaction medium, between a glyoxal of formula

wherein R 1 has the same meaning as defined above,

and an α-hydroxy ketone of formula

wherein R 1 has the same meaning as defined above,

in the presence of catalyst of formula FeX 3 or MX 2 , wherein M is Zn 2+ , Mg 2+ , Cu 2+ , Fe 2+ or Ca 2+ and X is a C 1 -C 7 carboxylate, an halide or an acetylacetonate derivative of formula (R 2 COCHCOR 2 ) − , R 2 representing a C 1 -C 3 alkyl group or a phenyl group.

According to a particular embodiment of the invention, R 1 represents a methyl group and therefore the glyoxal (II) is methyl glyoxal, the acetol (III) is acetol (i.e. 1-hydroxy-2-propanone) and the dihydroxy-dione (I) is 3,4-dihydroxyhexane-2,5-dione.

As mentioned above, the reaction is carried out in a water-containing reaction medium. By “water-containing reaction medium” it is meant here the medium wherein the reaction takes place, said medium containing at least 10% of water, percentage being relative to its own weight. In general the reaction medium comprises also an organic solvent, which can be water miscible or not. In general, any solvent which is inert under the experimental conditions is useful. In a particular embodiment of the invention, such a solvent is an ether or an ester such as tetrahydrofurane (THF), methyl-tert-butyl ether (MTBE) or ethylacetate.

As the process of the invention takes place in a water-containing reaction medium the pH of the solution has great importance for the course of the reaction. In that respect, we have discovered that, in order to ensure higher yields of compound (I), it is more advantageous to perform the invention's process in a weakly acidic to neutral medium.

According to an embodiment of the invention the present process is preferably carried out in a reaction medium having a pH of between 3.5 and 7, preferably between 4 and 6.5.

According to a particular embodiment of the invention the catalysts are the ones of formula MX 2 , wherein M is Zn 2+ or Mg 2+ , and X is an acetate, propionate, fluoride or acac, i.e., (CH 3 COCHCOCH 3 ) − . In particular, and as non-limiting examples of suitable catalyst, one can cite in particular Zn(acetate) 2 , Zn(acac) 2 , ZnF 2 or Mg(acac) 2 .

According to a further embodiment of the invention one may cite as catalysts ZnX 2 , wherein X represents a C 1 -C 3 carboxylate, such as Zn(acetate) 2 .

The amount in which the catalyst may be employed in the invention's process is typically comprised between 0.01 and 20 molar %, relative to the glyoxal. In a preferred embodiment of the process of the invention the catalyst is used in a concentration comprised between about 0.02 and 15 molar %.

The amount in which the acetol derivative (III) may be employed in the invention's process is typically comprised between 50 and 250 molar %, relative to the glyoxal.

The temperature at which the process of the invention can be carried out is comprised between 0° C. and 100° C., more preferably between 20° C. and 60° C.

›EXAMPLES

The invention will now be described in further detail by way of the following example, wherein the temperatures are indicated in degrees centigrade and the abbreviations have the usual meaning in the art.

›Example 1

Experimental Procedure

A solution of methyl glyoxal 40% wt in water (9 g, 50 mmoles), zinc acetate (0.44 g) and hydroxy-acetone (7.4 g) in ethyl acetate (20 ml) were stirred during 40 h at 38/40° (pH of the reaction medium was around 4.5). At the end of the reaction (which can be checked by gas chromatography), the reaction mixture was extracted with ethyl acetate (3×50 ml). The organic phase was washed to neutral with brine (1×), dried over magnesium sulphate and concentrated under vacuum giving 6 g of the crude 3,4-dihydroxyhexane-2,5-dione who was Bulb-to-bulb distilled at 0.1 mbar and 120-150° to obtain 3.8 g of a mixture of the two 3,4-dihydroxyhexane-2,5-dione isomers.

The product obtained had the same 1 H-NMR spectra as those described in Büchi et al, J. Org. Chem., 1973, 38, 123.

Following the same experimental procedure as above several other experiments according to the invention were performed. The results are summarized in the Table 1.

›Tables in the description — 1
TABLE 1 — Aldol condensation between methyl glyoxal and acetol to provide 3,4-dihydroxyhexane-2,5-dione, threo and meso isomers (2:1)
GlyoxalAcetolSolventTTimeCatalyst
N°(mmol.)(m.e.) 1)(ml)pH(° C.)(h)(m.e.) 1)yield
1505THF7.020°60Zn(acac) 220%
(20)(0.08)
2502.5H 2 O5.820°72Zn(acac) 220%
(20)(0.08)
3502EtOAc4.720°168Zn(acetate) 242%
(20)(0.04)
4502EtOAc4.540°40Zn(acetate) 232%
(20)(0.04)
5502EtOAc4.540°9Zn(acetate) 230%
(20)(0.10)
6505EtOAc2.640°24Zn(acetate) 222%
(20)(0.10)
7502EtOAc4.720°168ZnF 225%
(20)(0.04)
8502EtOAc5.520°168Mg(acetate) 218%
(20)(0.04)
9502EtOAc20°216Mg(acac) 223%
(20)(0.04)
m.e. = molar equivalent;
1) relative to methyl glyoxal

Claims as granted

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Classifications

3 codes
IPC · International Patent Classification
Section C — Chemistry; metallurgy
  • C07C45/72
USPC · US Patent Classification
568/390568/392

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Examiner
Sikarl A. Witherspoon
art unit 1621 · TC 1600
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