1.ApplicationNumber: US-7476660-A
1.PublishNumber: US-3082243-A
2.Date Publish: 19630319
3.Inventor: DAVIS HERMAN E.
JR. VINTON A. HOYLE,

4.Inventor Harmonized: DAVIS HERMAN E()
HOYLE JR VINTON A()

5.Country: US
6.Claims:

7.Description:
(en)Unite ates Patnt 3,082,243 Patented Mar. 19, 1963 3,082,243 UNSATURATED ESTERS F 2,2,4-TR1METHYL 1,3-?ENTANEDEOL MONOISOBUTYRATE Herman E. Davis and Vinton A. Hoyle, In, Kingsport,
Tenn, assignors to Eastman Kodak Company, Rochester, N.Y., a corporation of New Jersey No Drawing. Filed Dec. 9, 1960, Ser. No. 74,766 4 Claims. (Cl. 260-486) This invention relates to novel polymerizable monomeric materials. In particular it relates to esters of 2,2,4-trimethyl 1,3-pentanediol monoisobutyrate with colt-unsaturated monocarboxylic acids. These esters have utility in the preparation of new and useful homopolymers and copolymers for the plastic industry. Theproducts of the invention can be prepared by re acting 2,2,4-trimethyl 1,3-pentanediol monoisobutyrate with an a,B-unsaturated aliphatic monocarboxylic acid such as acrylic acid, methacrylic acid, or crotonic acid, following the usual procedures for preparing unsaturated esters. One suitable method is to reflux the 2,2,4-trimethyl .l,3-pentancdiol monoisobutyrate with a slight excess of the unsaturated acid in the presence of an esterification catalyst, a polymerization inhibitor, and an azeotroping solvent such as benzene or toluene. The mixture is refluxed and water formed by esterification is removed azeotropically. The catalyst and the azeotroping solvent are then removed and the product is purified by dis tillation. By this procedure we obtain a colorless mobile liquid of the following formula:
i E CH;OH-CHCCH2OR OR OHa wherein one of the Rs is the isobutyryl radical,
CH3 0 OHa-CH-(J- and the other is the acyl radical of an nap-unsaturated aliphatic monocarboxylic acid, such as 0113 O O CH2=OH l-, or OH2=C or CH3CH=CH(L) The two diiferent types of acyl radicals, R, are interchangeable in position but the molecule must contain one of each type. In other words, these are mixed esters that contain one unsaturated acyl substituent and one saturated acyl substituent, i.e., isobutyryl.
The starting material, 2,2,4-trimethy1 1,3-pentanediol monoisobutyrate, can be prepared by the self-condensation of isobutyraldehyde according to known procedures. See, for example, the paper by Kulpinski and Nord, J. Org. Chem., 8, 256, 268 (1943). The conditions of the condensation can be adjusted so that the product is either 2,2,4-trimethyl 1,3 pentanediol l-iso'butyrate or 2,2,4-trimethyl 1,3-pentanediol 3-isobutyrate or a mixture of the two isomers. Either isomer or a mixture of the two can be used as starting materials for preparing the mixed unsaturated esters of the invention.
The monomeric unsaturated esters of our invention have been polymerized by the Redox Emulsion technique and by bulk polymerization to give tough, flexible polymers. The polymers so formed are useful as viscosity improvers for lubricating oils and in plastic molding formulations. These monomers may also be copolymerized with other monomers such as methyl methacry-late, styrene, vinyl acetate, acrylonitrile, methacrylo nitrile, and other typical vinyl monomers. These copolymerizations take place in good yield. The ratio of each monomer may be varied in order to obtain the desired polymer properties.
The following examples illustrate the invention.
Example 1 To a 1-liter round-bottom flask equipped with a stirrer, Dean-Stark trap, reflux condenser, and thermometer were added one mole (216 g.) of 2,2,4-trimethyl 1,-3- pentanediol monoisobutyrate, 1.2 moles (103 g.) of methacrylic acid, 12 g. of p-toluenesulfonic acid, 200 ml. of benzene, 0.1 g. of methylene blue, and 0.1- g. of hydroquinone. This mixture was then refluxed for 7 hours whereupon 18 ml. of water was collected. The catalyst and excess methacrylic acid were then neutralized with a saturated sodium bicarbonate solution. The solution was washed with water until neutral, inhibited with 1 g. of hydroquinone and the benzene removed by distilla tion. On continued distillation of the crude product through a 20 plate packed column there was obtained a fraction boiling at -92 C. under 0.1-0.3 mm. pressure. This gave 250 g. of a water white liquid.
The 2,2,4-trimethy-l 1,3-pentanediol monoisobutyrate methacrylate obtained in Example I was emulsion polymerized by the following procedure. A mixture of 50 g. of the 2,2,4-trimethyl 1,3-pentanediol monoisobutyrate methacrylate, 250 g. of water, 1.25 g. of Duponol ME (2.5%), 0.5 g. of ammonium persulfate, and' 0.38 g. of sodium meta bisulfite was placed in a polymerization bottle, the air replaced with nitrogen and the bottle capped. The mixture was agitated for 24 hours at 40 C. .After breaking the emulsion, the polymer was recovered by filtration, and then washed thoroughly with warm water to remove all traces of catalyst and emulsifying agent. The dried polymer weighed 44.0 g. (88.0% yield). This material was soluble in benzene, toluene and chloroform, and insoluble in acetone, ethyl acetate, and the lower alcohols. This powder was molded into a tough plastic button at 250 F. (Duponol ME, a product of E. -I. du Pont de Nemours & Co., is a fatty alcohol sulfate emulsifying agent.)
The monomer was also copolymerized with methyl methacrylate using the same procedure as described above except that one-half of the 2,2,4-trimethyl 1,3-pentanediol monoisobutyrate methacrylate was replaced with methyl methacryate. A 96.4% yield of the copolymer was obtained. This product gave a somewhat rigid button when molded.
The 2,2,4-trimethyl 1,3-pentanediol monoisobutyrate methacrylate was copolymerized with acrylonitrile and meth-acrylonitrile in yields in excess of 90%.
Example 2 To a 1 liter round-bottom flask equipped with a thermometer, 18 inch distillation column packed with copper shavings, and a distillation head was added the following: 216 g. (1 mole) of 2,2,4-trimethy1 1,3-pentanediol monoisobutyrate, 12 g. p-toluenesulfonic acid, 15 g. of hydroquinone, 5 g. methylene blue, and 400 g. (4 moles) of ethyl acrylate. The mixture was refluxed until the ethanol-ethyl acrylate azeotrope began to form in the distillation head (evidenced by the boiling point, 77 C.). The azeotrope containing the ethanol was slowly removed as it was formed. The catalyst was neutralized with a saturated sodium bicarbonate solution and then and the other R is the excess ethyl acrylate was removed by distillation under reduced pressure. The colorless product was then CH O 3 distilled. I H
The invention has been described in detail with particu- CH3"CHC lar reference to preferred embodiments thereof, but it will be understood that variations and modifications can 2, The mixed ester 2,2,4-trimetl1y1 1,3-pentanedio1 be effected within the spirit and scope of the invention monoisgbutyrate methacrylate, as described hereinabove and as defined in the appended 3, Th mi ed ester 2,2,4-t1-imethy1 1,3-pentanedio1 claims. 10 monoisobutyrate crotonate.
We claim: 4. The mixed ester 2,2,4-trimethyl 1,3-pentanedio1 1. Esters of the formula monoisobutyrate acrylate.
' CH3 CH3 4 References Cited in the file of th1s patent CH3- H-CH CH:OR
OR CH 15 UNITED STATES PATENTS s 0 wherein one R is a radical selected from the group con- 2691663 Smlth 1954 slstmg 0f OTHER REFERENCES E i 20 Klupinski: Journal of Organic Chemistry, 1943, vol. CHz=CH-C, on,- -o--, and oH=-oH=011-o 8, PP- 256 Q 241