77889-21-5

Upstream product

• 4152-09-4 N-benzylethylenediamine 
• 6096-36-2 1-benzyl-2-methyl-4,5-dihydro-1H-imidazole 
• 629-27-6 1-Iodooctane 

Downstream Products

• 77889-27-1 1-benzyl-2-(1-propan-2-ylnonyl)-4,5-dihydroimidazole 
• 77889-26-0 1-benzyl-2-(1-butylnonyl)-4,5-dihydroimidazole 
• 106050-73-1 1-benzyl-2-(3-hydroxybutyl)-4,5-dihydroimidazole 
• 112-31-2 caprinaldehyde 
• 112-12-9 methyl nonyl ketone 
• 6048-82-4 decanophenone 
• 82462-00-8 N¹-benzyl-N¹-decyl-N²-methylethane-1,2-diamine 
• 109386-66-5 1-benzyl-3-methyl-2-nonyl-2,3,4,5-tetrahydroimidazole 
• 82461-99-2 N'-Benzyl-N-decyl-N-methyl-ethane-1,2-diamine 
• 31857-89-3 tetradecan-5-one 
• 82461-95-8 1-benzyl-3-methyl-2-nonyl-4,5-dihydroimidazolium iodide 
• 77889-25-9 1-benzyl-2-(1-methylnonyl)-4,5-dihydroimidazole 
• 106050-78-6 N-(2-benzylaminoethyl)decylamide 
• 82462-01-9 N¹-benzyl-N²-decylethane-1,2-diamine 

Relevant academic research and scientific papers

Nucleophilic Addition to 4,5-Dihydroimidazoles: A Ketone Synthesis via Tetrahydrofolate Coenzyme Models

1-Benzyl-2-alkyl-3-methyl-4,5-dihydroimidazolium salts with Grignard reagents give addition products that are hydrolysed to ketones; 4,5-dihydroimidazoles and 4,5-dihydroimidazolium salts with hydride reagents afford N-alkylated ethane-1,2-diamines.

Dihydroimidazoles in Synthesis: C-Alkylation of 1-Benzyl-2-(α-lithioalkyl)-4,5-dihydroimidazoles and a Synthesis of Alkanoic Acids

1-Benzyl-2-alkyl-4,5-dihydroimidazoles have been (laterally) metallated and C-alkylated by reaction with alkyl halides and an epoxide; intramolecular C-alkylation has led to a tetrahydro-5H-pyrroloimidazole.Hydrolysis of the 4,5-dihydroimidazoles to produce alkanoic acids completes a homologation sequence.