Vasickova, Sona; Tichy, Milos published an article on February 28 ,1979. The article was titled 《Stereochemical studies. LXXXVIII. Infrared spectra and conformation of substituted methyl cyclohexanecarboxylates and 2-hydroxycyclohexanecarboxylates》, and you may find the article in Collection of Czechoslovak Chemical Communications.Synthetic Route of C8H14O3 The information in the text is summarized as follows:
The IR of the C:O and OH groups in thirty-two Me alkylcyclohexane- and alkyl-trans-decalin-2-carboxylates and their vicinal OH derivatives were computer assigned to the appropriate conformers. The conformational equilibrium thermodn. and attractive interaction between equatorial OH and equatorial CO2Me groups were calculated in Me trans-2-hydroxy-cis-4-isopropylcyclohexanecarboxylate.Cis-methyl 2-hydroxycyclohexanecarboxylate(cas: 936-03-8Synthetic Route of C8H14O3) was used in this study.
Cis-methyl 2-hydroxycyclohexanecarboxylate(cas: 936-03-8) belongs to esters. 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. Synthetic Route of C8H14O3
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics