Selective Synthesis of Glyceryl Tris[9, 10‐(threo)‐dihydroxyoctadecanoate]. (6th July 2013)

• Record Type: Journal Article
• Authors: Elkin, Igor; Hildgen, Patrice
• Is Part Of: Journal of the American Oil Chemists' Society. Volume 90:Number 10(2013)
• Page Start: 1465
• Page End: 1474
• Publication Date: 2013-07-06
• Subjects: Glyceryl tris[9, 10‐(threo)‐dihydroxyoctadecanoate] -- Glyceryl trioleate -- Olive oil -- Hydroxy‐oxyformylation -- Deformylation; Oils and fats -- Periodicals; Soap -- Periodicals; Fats -- Periodicals; Food-Processing Industry -- Periodicals; Acides gras -- Périodiques; Aliments -- Industrie et commerce -- Périodiques; Huiles et graisses -- Périodiques; Savon -- Périodiques; Oliën; Chemie; Oils and fats; Soap; Periodicals; 547.77
• DOI: 10.1007/s11746-013-2295-z
• Languages: English
• ISSNs: 0003-021X

Abstract

Abstract: Elaborating novel triacylglyceride (TAG) based polyester hyperbranched unimolecular encapsulating agents represents an original and promising approach to the selective delivery of hydrophobic biologically active compounds. However, selective modification of double bonds in unsaturated TAG to obtain corresponding pure polyhydroxy derivatives with high yields is still a big challenge. Two novel approaches to synthesize the glyceryl tris[9, 10‐( threo )‐dihydroxyoctadecanoate] were proposed and tested: (1) via the bromination and nucleophilic substitution of secondary halide functions by oxyacetyl groups followed by the hydrolysis of acetyls, and (2) direct transformation of the double bonds by the reaction with peroxoformic acid in an excess of formic acid, and the removal of formyl protective groups. Glycerol trioleate and natural olive oil were used as starting materials. The first synthetic route allowed for successful preparation of the corresponding polyhalide and polyoxyacetyl products; however, a more effective final deacetylation procedure is required. The second proposed approach showed a very good reproducibility in obtaining hydroxy‐oxyformyl derivatives. The optimal conditions of the reaction involve the use of diethyl ether as a cosolvent and stirring at room temperature for 30 min. To remove the formyl groups, three original procedures using organic solvent medium at room temperature were proposed: in the presence of cesium carbonate in chloroform–methanol mixture, and two methods using hydrochloric acid in chloroform–methanol mixture or in acetone. All three methods were efficient to carry out the deformylation; nevertheless, TAG esters remained stable only with 15–17 % hydrochloric acid in acetone. Simple isolation procedures and high overall yields (95.6 and 94.9 % for both triolein and olive oil, respectively) allow considering the second approach as a promising method to obtain threo ‐polyhydroxy derivatives from unsaturated TAG.