Possible use of turpentine for the production of terpin hydrate, terpineol and their derivatives was written by Nikolin, A.;Petrovic, Z.;Vrcevic, J.;Nikolin, B.. And the article was included in Glasnik Hemicara i Tehnologa Bosne i Hercegovine in 1977.Electric Literature of C10H22O3 This article mentions the following:
Terpin hydrate (I) [2451-01-6] and α-terpineol (II) [98-55-5] are prepared from turpentine oil without a preliminary separation of I and used for preparation of esters and ethers with various fatty acids and alkyl iodides, resp. Turpentine oil containing 60-85% pinene fraction was converted to I, II, and fatty acid esters. A 72% II was prepared by dehydration of I with H3PO4. α-Terpineol acetate [80-26-2] was prepared by addition of 100 g turpentine oil, in 5 mL portions, to a mixture of 200 g AcOH and 10 mL 50% H2SO4 at 30° and 1 h standing at room temperature Diacetate and diformate of I were prepared by the reaction of I with Ac2O and HCO2H. In the experiment, the researchers used many compounds, for example, rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate (cas: 2451-01-6Electric Literature of C10H22O3).
rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate (cas: 2451-01-6) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. Secondary alcohols are easily oxidized without breaking carbon-carbon bonds only as far as the ketone stage. No further oxidation is seen except under very stringent conditions.Electric Literature of C10H22O3
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts