(en)Processes for refining dialkyl carbonate-containing compositions are described, wherein a composition comprising a dialkyl carbonate is provided; and the composition is subjected to a rectification wherein low-boiling impurities are removed, and a rectification wherein high-boiling impurities are removed; and subsequently to a deodorization wherein medium-boiling impurities are removed.

1.ApplicationNumber: US-48761504-A
1.PublishNumber: US-7094917-B2
2.Date Publish: 20060822
3.Inventor: RIDINGER RICHARD
YUEKSEL LEVENT
FIEG GEORG

4.Inventor Harmonized: RIDINGER RICHARD(DE)
YUEKSEL LEVENT(DE)
FIEG GEORG(DE)

5.Country: US
6.Claims:
(en)Processes for refining dialkyl carbonate-containing compositions are described, wherein a composition comprising a dialkyl carbonate is provided; and the composition is subjected to a rectification wherein low-boiling impurities are removed, and a rectification wherein high-boiling impurities are removed; and subsequently to a deodorization wherein medium-boiling impurities are removed.

7.Description:
(en)BACKGROUND OF THE INVENTION
Dialkyl carbonates are interesting new oil components for cosmetic products and are normally obtained by transesterification of dimethyl or diethyl carbonate with relatively long-chain fatty alcohols. Particular preference attaches to the production and use of dioctyl carbonate which is commercially available under the INCI name of Dicaprylyl Carbonate and the registered name of Cetiol® CC (Cognis Deutschland GmbH) [cf. WO 97/47583 (Cognis)]. Unfortunately, carbonates have the disadvantage of a “sweaty” odor so that perfuming is necessary where they are used in cosmetic products. The deodorization with steam normally applied in such cases has proved unsuccessful.
Accordingly, the problem addressed by the present invention was to provide dialkyl carbonates which would have an improved odor quality in relation to the prior art and which would therefore be suitable for use in cosmetic products.
BRIEF SUMMARY OF THE INVENTION
The present invention relates, in general, to the field of cosmetics and, more particularly, to a process for the production of oil components of the dialkyl carbonate type, in which products with improved odor properties are obtained.
The present invention relates to a process for the production of dialkyl carbonates corresponding to formula (I):

R 1 OCOOR 2 (I)

in which R 1 and R 2 independently of one another represent linear or branched hydrocarbon radicals containing 6 to 22 carbon atoms and 0 or 1 to 3 double bonds,

by transesterification of C 1-4 dialkyl carbonates with C 6-22 alcohols, characterized in that
(a) the crude transesterification mixture is subjected to a first rectification in which the low-boiling impurities are distilled off, (b) the “bottom” product thus obtained is subjected to a second rectification in which the high-boiling impurities are removed and (c) finally, in a deodorizing column, the distillate thus obtained is freed from medium-boiling impurities, more particularly odor carriers, either with steam or with inert gases.

The invention is based on the observation that the odor problem with dialkyl carbonates is attributable to very different impurities which can only be removed by different process measures. It has surprisingly been found that the combination of two rectification steps and one deodorization step ultimately yields a product which is satisfactory from the odor perspective and which may be used without additional perfuming in cosmetic products.


DETAILED DESCRIPTION OF THE INVENTION
Rectification
In the course of the two-stage rectification, the unwanted low-boiling impurities are removed in the first step. The bottom product is then subjected to a second rectification in which the high-boiling impurities are left in the bottom of the column and only the distillate is subsequently used. It has proved to be particularly advantageous—because less damage is done to the materials used—to evaporate the crude transesterification mixture and/or the distillate obtained as intermediate product in a combination of thin-layer and falling-film evaporators. The rectification itself is carried out in particular in columns with structured packings which preferably have a pressure loss of less than 1–2 mbar/m. The first rectification is normally carried out at temperatures (bottom) in the range from 180 to 250° C. and under a reduced pressure (head) of 0.01 to 10 mbar and preferably at temperatures (bottom) in the range from 180 to 200° C. and under a reduced pressure (head) of 1 to 10 mbar. The second rectification is normally carried out at temperatures (bottom) in the range from 150 to 250° C. and under a reduced pressure (head) of 0.01 to 0.5 mbar and preferably at temperatures (bottom) in the range from 150 to 180° C. and under a reduced pressure (head) of 0.01 to 0.5 mbar.
Deodorization
The deodorization is generally carried out in a column under a reduced pressure of 10 to 100 mbar using either steam or inert gases, preferably nitrogen.
EXAMPLE
The working up of a technical dioctyl carbonate was carried out in two coupled rectifying columns each with a 0.5 m EX packing (Sulzer AG) and a deodorizing column. The column diameters were 30 mm. The crude transesterification mixture was evaporated in a combination of thin-layer and falling-film evaporators and delivered to the first rectifying column where the head pressure was 5 mbar, the bottom temperature 185° C., the pressure loss ca. 9 mbar and the reflux ratio 5. 43.5% by weight low-boiling distillate and 56.5% by weight valuable product were obtained at the bottom of the column. The bottom product was then evaporated in the same way and delivered to the second rectifying column where the head pressure was 0.1 mbar, the bottom temperature 176° C., the pressure loss ca. 9 mbar and the reflux ratio 3. The subsequent deodorization was carried out with nitrogen at 100° C. in a separate column. The product obtained was completely odorless, even after storage for 6 months.
FIG. 1 is a flow chart of the process.