N,N-Dicyclobutylbenzylamine

Base Information

• Chemical Name: N,N-Dicyclobutylbenzylamine
• CAS No.: 177721-42-5
• Molecular Formula: C₁₅H₂₁N
• Molecular Weight: 215.338
• DSSTox Substance ID: DTXSID50440755
• Nikkaji Number: J744.816C
• Wikidata: Q82257150
• Mol file: 177721-42-5.mol

Synonyms:N,N-DICYCLOBUTYLBENZYLAMINE;177721-42-5;N-benzyl-N-cyclobutylcyclobutanamine;DTXSID50440755;Quinonimine, 2,6-dibromo-N-chloro-

Chemical Property of N,N-Dicyclobutylbenzylamine

Chemical Property:

• Boiling Point: 309.4±11.0 °C(Predicted)
• PKA: 10.08±0.20(Predicted)
• PSA: 3.24000
• Density: 1.03±0.1 g/cm3(Predicted)
• LogP: 3.59360
• XLogP3: 3.6
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 4
• Exact Mass: 215.167399674
• Heavy Atom Count: 16
• Complexity: 198

Purity/Quality:

N,N-DICYCLOBUTYLBENZYLAMINE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CC(C1)N(CC2=CC=CC=C2)C3CCC3

Technology Process of N,N-Dicyclobutylbenzylamine

There total 4 articles about N,N-Dicyclobutylbenzylamine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

cyclobutanone (1191-95-3) + benzylamine (100-46-9) → N,N-dicyclobutylbenzylamine (177721-42-5)

Guidance literature:

With sodium tris(acetoxy)borohydride; acetic acid; In 1,2-dichloro-ethane; for 2h; Ambient temperature;

DOI:10.1021/jo960057x

Reference yield:

hexamethylene imine (111-49-9) + cyclopentanone (120-92-3) → N-cyclopentylhexamethyleneimine (5024-91-9) + N,N-dicyclobutylbenzylamine (177721-42-5)

Guidance literature:

With sodium tris(acetoxy)borohydride; acetic acid; In 1,2-dichloro-ethane; for 24h; Yields of byproduct given; Ambient temperature;

DOI:10.1021/jo960057x

Reference yield:

4-phenyl-1-piperazine (92-54-6) + cyclobutanone (1191-95-3) → N,N-dicyclobutylbenzylamine (177721-42-5) + 1-cyclobutyl-4-phenylpiperazine

Guidance literature:

With sodium tris(acetoxy)borohydride; In 1,2-dichloro-ethane; for 2h; Yields of byproduct given; Ambient temperature;

DOI:10.1021/jo960057x

upstream raw materials:

hexamethylene imine

cyclopentanone

4-phenyl-1-piperazine

cyclobutanone

Refernces