Crotyl

You don't need to be Editor-In-Chief to add or edit content to WikiDoc. You can begin to add to or edit text on this WikiDoc page by clicking on the edit button at the top of this page. Next enter or edit the information that you would like to appear here. Once you are done editing, scroll down and click the Save page button at the bottom of the page.

A crotyl group is an organic functional group with the formula CH₂CH=CHCH₃. Systematically, it is called a 2-butenyl group and exhibits geometric isomerism, being either cis (Z) or trans (E). There are many simple compounds in which the crotyl group forms base carbon chain: crotyl alcohol, crotonaldehyde, crotonic acid, and crotyl acrylate are examples.

Synthesis of crotylates

Crotylate (crotyl anions) can be synthesised from 2-butene (either isomer) with organometallic reagents, usually alkyl lithium, and alkylates of s-block metals. This reaction must be performs in the presence of a base, typically THF, and at low temperatures, generally below -20°C. The negative charge is delocalised over three of the carbon atoms of the crotylate group and there is resonance between the two possible delocalised forms (one for each terminal carbon).

Crotylation reactions

Crotylation readily occurs with alkoxy boronates to form crotylboronates.

Crotylboronates are useful reagents in the formation of crotyl alcohols. They react with the acidic protons of aldehydes to form alcohols. The mechanism involves a six-membered ring involving the carbonyl oxygen and boron in a chair-like structure. Such reactions are highly diastereoselective