Synthesis of 2,2-dimethyl-5-hydroxymethyl-1,3-dioxane was written by Li, Peijie;Xu, Zheng;Wu, Xiaochun;Wu, Yong. And the article was included in Huaxi Yaoxue Zazhi in 2001.Name: Ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate This article mentions the following:
2,2-Dimethyl-5-hydromethyl-1,3-dioxane was synthesized from di-Et malonate by condensation with formaldehyde in the presence of KHCO3, further condensation with 2,2-dimethoxypropane, decarboxylation in DMSO-NaCl, and reduction with LiAlH4, provide product with over all yield 41%. In the experiment, the researchers used many compounds, for example, Ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate (cas: 82962-54-7Name: Ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate).
Ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate (cas: 82962-54-7) belongs to esters. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Polyesters are important plastics, with monomers linked by ester moieties. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Name: Ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics