N-Benzyl-N-(2-bromophenyl)acetamide

Base Information

Chemical Name:N-Benzyl-N-(2-bromophenyl)acetamide
CAS No.:111022-42-5
Molecular Formula:C₁₅H₁₄BrNO
Molecular Weight:304.186
Hs Code.:
DSSTox Substance ID:DTXSID40578738
Nikkaji Number:J1.009.386D
Wikidata:Q82469051
Mol file:111022-42-5.mol

Synonyms:N-Benzyl-N-(2-bromophenyl)acetamide;111022-42-5;DTXSID40578738

Suppliers and Price of N-Benzyl-N-(2-bromophenyl)acetamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of N-Benzyl-N-(2-bromophenyl)acetamide

Chemical Property:

XLogP3:3.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:303.02588
Heavy Atom Count:18
Complexity:276

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)N(CC1=CC=CC=C1)C2=CC=CC=C2Br

Technology Process of N-Benzyl-N-(2-bromophenyl)acetamide

There total 4 articles about N-Benzyl-N-(2-bromophenyl)acetamide 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: 35.0%

: 876061-26-6
N-benzyl-2-bromo-N-(2-bromophenyl)acetamide

: 1663-39-4,25232-27-3
tert-Butyl acrylate

: tert-butyl 2-(1-benzyl-2-oxo-1,2,3,4-tetrahydroquinolin-4-yl)acetate

: 111022-42-5
N-benzyl-N-(2-bromophenyl)acetamide

Guidance literature:: Multistep reaction. Title compound not separated from byproducts;
DOI:10.1021/ol052730n

Reference yield:

: 71687-81-5
N-benzyl-2-bromoaniline

: 111022-42-5
N-benzyl-N-(2-bromophenyl)acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / triethylamine / CH₂Cl₂ / 20 °C

With triethylamine; In dichloromethane;
DOI:10.1021/ol052730n

Reference yield:

: 615-36-1
2-bromoaniline

: 111022-42-5
N-benzyl-N-(2-bromophenyl)acetamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: triethylamine / tetrahydrofuran / 0.67 h / 0 - 20 °C

2.1: sodium hydride / tetrahydrofuran / 0.67 h / 0 °C

2.2: 0 - 20 °C

With sodium hydride; triethylamine; In tetrahydrofuran;
DOI:10.1016/j.mcat.2022.112211