N-[(2-Bromophenyl)methyl]-2-methylpropan-2-amine

Base Information

• Chemical Name: N-[(2-Bromophenyl)methyl]-2-methylpropan-2-amine
• CAS No.: 356531-35-6
• Molecular Formula: C11H16BrN
• Molecular Weight: 242.159
• Hs Code.: 2921499090
• DSSTox Substance ID: DTXSID80460946
• Wikidata: Q82285137
• Mol file: 356531-35-6.mol

Synonyms:356531-35-6;N-[(2-Bromophenyl)methyl]-2-methylpropan-2-amine;N-(2-BROMOPHENYLMETHYL)TERT-BUTYLAMINE;Oprea1_439518;DTXSID80460946;AKOS000190832;[(2-bromophenyl)methyl](tert-butyl)amine;EN300-58139;C78163;AB00999692-01

Chemical Property of N-[(2-Bromophenyl)methyl]-2-methylpropan-2-amine

Chemical Property:

• PSA: 12.03000
• LogP: 3.72810
• XLogP3: 3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 241.04661
• Heavy Atom Count: 13
• Complexity: 151

Purity/Quality:

98.5% ^*data from raw suppliers

[(2-BROMOPHENYL)METHYL](TERT-BUTYL)AMINE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)(C)NCC1=CC=CC=C1Br

Technology Process of N-[(2-Bromophenyl)methyl]-2-methylpropan-2-amine

There total 2 articles about N-[(2-Bromophenyl)methyl]-2-methylpropan-2-amine 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:

N-(2-bromobenzylidene)-2-methylpropan-2-amine → N-(2-bromobenzyl)-2-methylpropan-2-amine (356531-35-6)

Guidance literature:

With sodium tetrahydroborate; In methanol; at 20 ℃; for 18h;

DOI:10.1021/ja038565t

Reference yield:

ortho-bromobenzaldehyde (6630-33-7) → N-(2-bromobenzyl)-2-methylpropan-2-amine (356531-35-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 4 A molecular sieves / toluene

2: 4.82 g / NaBH₄ / methanol / 18 h / 20 °C

With sodium tetrahydroborate; 4 A molecular sieve; In methanol; toluene;

DOI:10.1021/ja038565t

Reference yield: 90.0%

2-azetidinone (930-21-2) + N-(2-bromobenzyl)-2-methylpropan-2-amine (356531-35-6) → 5-tert-butyl-2,3,5,6-tetrahydro-1H-benzo[b][1,5]diazocin-4-one + 1-[2-(tert-butylaminomethyl)phenyl]-2-azetidinone

Guidance literature:

With copper(l) iodide; potassium carbonate; N,N`-dimethylethylenediamine; In toluene; at 110 ℃; for 23h;

DOI:10.1021/ja038565t

upstream raw materials:

ortho-bromobenzaldehyde