2-Acetamido-N-benzyl-2-(ethanesulfinyl)acetamide

Base Information

Chemical Name:2-Acetamido-N-benzyl-2-(ethanesulfinyl)acetamide
CAS No.:194732-66-6
Molecular Formula:C13H18N2O3S
Molecular Weight:282.364
Hs Code.:
ChEMBL ID:CHEMBL79316
DSSTox Substance ID:DTXSID60564774
Nikkaji Number:J421.146D

Synonyms:194732-66-6;2-Acetamido-N-benzyl-2-(ethanesulfinyl)acetamide;CHEMBL79316;SCHEMBL8837119;DTXSID60564774

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

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Chemical Property of 2-Acetamido-N-benzyl-2-(ethanesulfinyl)acetamide

Chemical Property:

XLogP3:0.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:282.10381361
Heavy Atom Count:19
Complexity:341

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCS(=O)C(C(=O)NCC1=CC=CC=C1)NC(=O)C

Technology Process of 2-Acetamido-N-benzyl-2-(ethanesulfinyl)acetamide

There total 3 articles about 2-Acetamido-N-benzyl-2-(ethanesulfinyl)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: 52.0%

: 133873-24-2
2-acetamido-N-benzyl-2-(ethylmercapto)acetamide

: 194732-66-6
2-Acetamido-N-benzyl-2-(ethylmercapto)acetamide-S-oxide

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at -15 - -10 ℃; for 0.5h;
DOI:10.1021/jm00112a020

Reference yield:

: 117422-80-7
α-acetamido-N-benzyl-α-ethoxyacetamide

: 194732-66-6
2-Acetamido-N-benzyl-2-(ethylmercapto)acetamide-S-oxide

Guidance literature:: Multi-step reaction with 3 steps

1: BBr₃ / CH₂Cl₂ / 5 h / Ambient temperature

2: Et₃N / tetrahydrofuran / 1.) -78 deg C, 30 min, 2.) RT, 1 h

3: NaIO₄ / H₂O; methanol / 4 h / Ambient temperature

With sodium periodate; boron tribromide; triethylamine; In tetrahydrofuran; methanol; dichloromethane; water;
DOI:10.1021/jm00112a020

Reference yield:

: 133873-18-4
α-acetamido-N-benzyl-α-bromoacetamide

: 194732-66-6
2-Acetamido-N-benzyl-2-(ethylmercapto)acetamide-S-oxide

Guidance literature:: Multi-step reaction with 2 steps

1: Et₃N / tetrahydrofuran / 1.) -78 deg C, 30 min, 2.) RT, 1 h

2: NaIO₄ / H₂O; methanol / 4 h / Ambient temperature

With sodium periodate; triethylamine; In tetrahydrofuran; methanol; water;
DOI:10.1021/jm00112a020