130655-17-3

Upstream product

• 130674-30-5 [2-(1-Butyl-cyclohex-2-enyloxy)-ethanesulfinyl]-benzene 
• 130655-10-6 2-(1-butylcyclohex-2-en-1-yloxy)ethyl p-chlorophenyl sulfoxide 
• 88116-46-5 1-butyl-2-cyclohexen-1-ol 

Relevant academic research and scientific papers

Preparation and rearrangement of 2-allyloxyethyl aryl sulfoxides; a mercury-free claisen sequence

Alkali metal hydride promoted addition of allylic alcohols to aryl vinyl sulfoxides at room temperature gives 2-allyloxyethyl aryl sulfoxides, which, on heating, are converted into γ,δ-unsaturated aldehydes via allylic vinyl ethers.