105452-90-2

Basic information

• Product Name: N-(octan-2-yl)benzamide
• CAS NO: 105452-90-2
• Molecular Weight: 233.354
• Mol File: 105452-90-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N-(octan-2-yl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(octan-2-yl)benzamide(105452-90-2)
• EPA Substance Registry System: N-(octan-2-yl)benzamide(105452-90-2)

Safety Data

• Hazardous Substances Data: 105452-90-2(Hazardous Substances Data)

Upstream product

• 44855-57-4 rac-2-aminooctane 
• 98-88-4 benzoyl chloride 
• 111-66-0 oct-1-ene 
• 55-21-0 benzamide 
• 53475-02-8 (R)-2-azido-octane 
• 34817-25-9 (S)-1-methylheptyl tosylate 
• 100-47-0 benzonitrile 
• 6169-06-8 (S)-2-Octanol 
• 693-16-3 (R)-2-octylamine 

Relevant articles and documents

Chiral 2-imidazoline aniline compound as well as preparation method and application thereof

The invention provides a chiral 2-imidazoline aniline compound as well as a preparation method and application thereof. The preparation method comprises the following steps: reacting an o-nitrobenzoic acid compound as shown in a formula (1), oxalyl chloride and N, N-dimethylformamide to obtain an o-nitrobenzoyl chloride compound as shown in a formula (7); adding the hydroxyl amide derivative into a mixed solution of an amino alcohol compound as shown in a formula (2) and triethylamine to obtain a hydroxyl amide derivative as shown in a formula (3); reacting with thionyl chloride to obtain a dichloro compound as shown in a formula (4); then adding triethylamine and primary amine R2NH2 to prepare a nitroimidazoline derivative; and finally, reducing to obtain the chiral 2-imidazoline aniline compound as shown in a formula (6). The chiral 2-imidazoline aniline compound is easy to prepare, the raw materials are cheap and easy to obtain, the preparation method is simple, and the synthesized chiral ligand containing the 2-imidazoline aniline fragment can be used as a catalyst for catalyzing asymmetric hydroboration reaction of cobalt-catalyzed olefin and asymmetric hydroamination reaction of cobalt-catalyzed non-activated terminal olefin.

Iridium-catalyzed intermolecular hydroamination of unactivated aliphatic alkenes with amides and sulfonamides

The intermolecular addition of N-H bonds to unactivated alkenes remains a challenging, but desirable, strategy for the synthesis of N-alkylamines. We report the intermolecular amination of unactivated α-olefins and bicycloalkenes with arylamides and sulfonamides to generate synthetically useful protected amine products in high yield. Mechanistic studies on this rare catalytic reaction revealed a resting state that is the product of N-H bond oxidative addition and coordination of the amide. Rapid, reversible dissociation of the amide precedes reaction with the alkene, but an intramolecular, kinetically significant rearrangement of the species occurs before this reaction with alkene.