2-bromo-N-phenyl-N-(phenylsulfonyl)acetamide

Base Information

Chemical Name:2-bromo-N-phenyl-N-(phenylsulfonyl)acetamide
CAS No.:145326-62-1
Molecular Formula:C₁₄H₁₂BrNO₃S
Molecular Weight:354.224
Hs Code.:
DSSTox Substance ID:DTXSID601257535

Synonyms:2-bromo-N-phenyl-N-(phenylsulfonyl)acetamide;145326-62-1;DTXSID601257535

Suppliers and Price of 2-bromo-N-phenyl-N-(phenylsulfonyl)acetamide

Supply Marketing:

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

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Chemical Property of 2-bromo-N-phenyl-N-(phenylsulfonyl)acetamide

Chemical Property:

XLogP3:3.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:352.97213
Heavy Atom Count:20
Complexity:420

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)N(C(=O)CBr)S(=O)(=O)C2=CC=CC=C2

Technology Process of 2-bromo-N-phenyl-N-(phenylsulfonyl)acetamide

There total 3 articles about 2-bromo-N-phenyl-N-(phenylsulfonyl)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:

: 1678-25-7
N-phenylbenzenesulfonamide

: 598-21-0
2-Bromoacetyl bromide

: 145326-62-1
2-bromo-N-phenyl-N-(phenylsulfonyl)acetamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In benzene; at 0 ℃; for 2h;
DOI:10.1080/00397919208021125

Reference yield:

: 62-53-3
aniline

: 145326-62-1
2-bromo-N-phenyl-N-(phenylsulfonyl)acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dichloromethane / 20 °C / Inert atmosphere; Schlenk technique

2: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C / Inert atmosphere; Schlenk technique

With triethylamine; N-ethyl-N,N-diisopropylamine; In dichloromethane;
DOI:10.1021/acs.joc.6b00735

Reference yield:

: 98-09-9
benzenesulfonyl chloride

: 145326-62-1
2-bromo-N-phenyl-N-(phenylsulfonyl)acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dichloromethane / 20 °C / Inert atmosphere; Schlenk technique

2: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C / Inert atmosphere; Schlenk technique

With triethylamine; N-ethyl-N,N-diisopropylamine; In dichloromethane;
DOI:10.1021/acs.joc.6b00735