Production of α-terpineol from α-pinene was written by Benkli, Kadriye;Isikdag, Ilhan;Baser, K. Husnu Can. And the article was included in Acta Pharmaceutica Turcica in 1995.Product Details of 2451-01-6 This article mentions the following:
α-Terpineol (I) is a monoterpenic alc. used as a fragrance material in the perfumery industry and for the production of some volatile compounds Several techniques have been described in the literature for its synthesis. These techniques recommend the conversion of olefinic terpenes to their hydrochlorides or esters with acids, followed by hydrolysis into the desired alc. This paper describes a method which involves hydration of α-pinene (II) to terpinhydrate which is then dehydrated to give I. Cation exchange resin was also used in an oxygen-free medium to obtain I in higher (73%) yield from II. In the experiment, the researchers used many compounds, for example, rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate (cas: 2451-01-6Product Details of 2451-01-6).
rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate (cas: 2451-01-6) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. Under carefully controlled conditions, simple alcohols can undergo intermolecular dehydration to give ethers. This reaction is effective only with methanol, ethanol, and other simple primary alcohols.Product Details of 2451-01-6
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts