Publication Cover
Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 10, 1980 - Issue 3
64
Views
14
CrossRef citations to date
0
Altmetric
Original Articles

Isomerization of Estragole to Anethole

Pages 225-231 | Published online: 05 Dec 2006
 

Abstract

Anethole (trans-isomer, I) is an industrially significant organic which has found use predominantly as a flavor and fragrance (licorice) chemical. I is a component of many essential oils, e.g., fennel oils, from which it is isolated for application. Rather than depending on natural sources in toto, in its wisdom the chemical industry has chosen to fortify availability through chemical synthesis. An accepted route1 involves the isomerization of estragole (II) to I with strong base at 200° for an extended2 time period.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.