Synthesis of rac-bisabola-3(15),10-dien-7-ol was written by Weyerstahl, Peter;Schlicht, Volker. And the article was included in Liebigs Annalen/Recueil in 1997.Recommanded Product: Ethyl 4-methylenecyclohexanecarboxylate This article mentions the following:
1-Acetyl-4-methylenecyclohexane was obtained from 4-methylenecyclohexanecarboxylate, by DIBAH reduction, Grignard reaction, and oxidation A further Grignard reaction furnished rac-bisabola-3(15),10-dien-7-ol, which was isolated recently from vetiver oil. Its odor is mainly aldehydic (fatty, floral). In the experiment, the researchers used many compounds, for example, Ethyl 4-methylenecyclohexanecarboxylate (cas: 145576-28-9Recommanded Product: Ethyl 4-methylenecyclohexanecarboxylate).
Ethyl 4-methylenecyclohexanecarboxylate (cas: 145576-28-9) belongs to esters. Volatile esters with characteristic odours are used in synthetic flavours, perfumes, and cosmetics. Certain volatile esters are used as solvents for lacquers, paints, and varnishes. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.Recommanded Product: Ethyl 4-methylenecyclohexanecarboxylate
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics