Related Experiment Video
Updated: Sep 18, 2025

Preparation of Enantiopure Non-Activated Aziridines and Synthesis of Biemamide B, D, and epiallo-Isomuscarine
Published on: June 13, 2022
From Turpentine to (-)-Menthol: A New Approach
Matthias Eisenacher1, Dominik Dylong2, Johannes Panten2
1Circular Transformation Lab, TH Köln-University of Applied Sciences, Campusplatz 1, 51379, Leverkusen, Germany.
None:
The rising popularity of (-)-menthol, as the main component of the natural mint aroma with applications in the pharmaceuticals, cosmetics, and food industries leads to a growing need for synthetic menthol production to satisfy the world demand. In this study, a novel green synthesis route for menthol is presented. The proposed method utilizes renewable starting materials and employs environmentally benign reaction conditions, making it an attractive alternative to conventional menthol synthesis methods. The starting material, 3-carene, which can be obtained by distillation from crude sulfate turpentine, is transformed via heterogeneous hydrogenation and heterogeneous acidic isomerization to a mixture of unsaturated menthenes. The catalytic epoxidation of the menthenes with hydrogen peroxide and hydrogenation of the epoxides leads to a mixture of menthol isomers, which can be separated and recycled by established methods to obtain the desired (-)-menthol.
More Related Videos
08:56Transient Expression in Nicotiana Benthamiana Leaves for Triterpene Production at a Preparative Scale
Published on: August 16, 2018
05:34Efficient Synthesis of Polyfunctionalized Benzenes in Water via Persulfate-promoted Benzannulation of α,β-Unsaturated Compounds and Alkynes
Published on: December 16, 2019
Related Concept Videos
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Ethers from Alkenes: Alcohol Addition and Alkoxymercuration-Demercuration
Ethers can also be prepared from alkenes through acid-catalyzed addition of alcohols and alkoxymercuration–demercuration.
Preparation of Ethers by Acid-Catalyzed Addition of Alcohol to Alkenes
The acid-catalyzed addition of alcohol to an alkene involves treating the alkene with an excess of alcohol in the presence of an acid catalyst to form an ether under suitable conditions. The hydrogen will add to the less substituted carbon so that the nucleophile can attack the more...
Oxymercuration-Reduction of Alkenes
Hydroboration-Oxidation of Alkenes
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Alkenes via Reductive Coupling of Aldehydes or Ketones: McMurry Reaction