Odham, Goran; Pettersson, Bente; Stenhagen, Einar published the artcile< Use of optically active half-esters of methoxy-substituted succinic acids in the stereospecific synthesis of long chain oxygenated compounds>, Synthetic Route of 617-55-0, the main research area is tetradecanoate ester methoxy; chain lengthening malate ester; electrolytic chain lengthening lauric acid.
The isomeric half-esters of (S)-methoxysuccinic acid have been prepared in the search of suitable intermediates for the synthesis of the β-glycol group of phthiocerol. The half-esters have very similar properties and differ mainly in the mass spectra and ir spectra. Chain-lengthening of (S)-methyl 2-methoxy-3-carboxypropanoate by mixed electrolysis with dodecanoic acid in DMF gave a 21% yield of (S)-methyl 2-methoxytetradecanoate.
Acta Chemica Scandinavica, Series B: Organic Chemistry and Biochemistry published new progress about Coupling reaction. 617-55-0 belongs to class esters-buliding-blocks, and the molecular formula is C6H10O5, Synthetic Route of 617-55-0.
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics