41040-63-5

Usage

Class

The compound belongs to the class of alkynes and amines.

Molar mass

The molar mass of the compound is 155.28 g/mol.

Structure

The compound is made up of a pentyn-3-amine group, which consists of a five-carbon chain with a triple bond and an amino group attached to the third carbon.

Substituent

The compound has a N-butyl-3-methyl moiety, which refers to a butyl group (four-carbon chain) attached to the amino group with a methyl group (one carbon) attached to the third carbon atom of the butyl chain.

Potential uses

The compound has the potential to be used in various synthetic reactions and may have industrial applications.

Upstream product

• 1185-96-2 3-acetoxy-3-ethylbutyne 
• 109-73-9 N-butylamine 
• 10575-70-9 1-bromo-3-methyl-1,2-pentadiene 
• 77-75-8 meparfynol 

Relevant academic research and scientific papers

An unprecedented Pd-catalyzed, water-promoted sequential oxidative aminocarbonylation-cyclocarbonylation process leading to 2-oxazolidinones

An unprecedented, Pdl2-catalyzed, sequential oxidative aminocarbonylation-cyclocarbonylation process, leading to 2-oxazolidinone derivatives 3 in good to excellent yields starting from readily available α,α-disubstituted 2-ynylamines 1 and secondary amines 2, is reported. In the case of an α-monosubstituted substrate, the initially formed 2-oxazolidinone derivative underwent shift of the double bond to give a 3H-oxazol-2-one derivative in excellent isolated yield.

REACTIONS OF NITROGEN NUCLEOPHILES WITH 1-BROMOALLENES: REGIOSELECTIVE SYNTHESIS OF PROPARGYLAMINES

The results of a study on the reactivity of 3-alkyl- and 3,3-dialkyl-1-bromo-1,2-dienes 2 towards nitrogen nucleophiles, such as aqueous ammonia, lithium amide, aliphatic and aromatic amines allowed us to propose new methods for the synthesis of propargylamines, 1, with an available acetylenic hydrogen.The regio- and the stereoselectivity of these reactions are examined and possible mechanisms are discussed.

Copper Catalyzed Aminolysis of Bromoallenes as a New Efficient Route to Propargylamines

An efficient procedure of general applicability for the synthesis of secondary and tertiary propargylamines by copper mediated aminolysis of 1-bromo-1,2-dienes is described.Key Words: propargylamines; bromoallenes; aminolysis; regioselectivity; Cu promote