N-(3-Chlorophenyl)-N-[(methanesulfonyl)oxy]acetamide

Base Information

• Chemical Name: N-(3-Chlorophenyl)-N-[(methanesulfonyl)oxy]acetamide
• CAS No.: 88730-34-1
• Molecular Formula: C9H10ClNO4S
• Molecular Weight: 263.702
• DSSTox Substance ID: DTXSID30523176
• Wikidata: Q82389116

Synonyms:88730-34-1;N-(3-Chlorophenyl)-N-[(methanesulfonyl)oxy]acetamide;DTXSID30523176

Chemical Property of N-(3-Chlorophenyl)-N-[(methanesulfonyl)oxy]acetamide

Chemical Property:

• XLogP3: 1.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 263.0019067
• Heavy Atom Count: 16
• Complexity: 351

Purity/Quality:

85.0-99.8% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CC(=O)N(C1=CC(=CC=C1)Cl)OS(=O)(=O)C

Technology Process of N-(3-Chlorophenyl)-N-[(methanesulfonyl)oxy]acetamide

There total 2 articles about N-(3-Chlorophenyl)-N-[(methanesulfonyl)oxy]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:

N-(3-chlorophenyl)hydroxylamine (10468-17-4) → C9H10ClNO4S (88730-34-1)

Guidance literature:

Multi-step reaction with 2 steps

1: sodium bicarbonate / diethyl ether; H₂O / 0 °C

2: triethylamine / CH₂Cl₂ / below 0 deg C

With sodium hydrogencarbonate; triethylamine; In diethyl ether; dichloromethane; water;

DOI:10.1021/ja00317a060

Reference yield:

N-(3-chlorophenyl)-N-hydroxyacetamide (88730-41-0) + methanesulfonyl chloride (124-63-0) → C9H10ClNO4S (88730-34-1)

Guidance literature:

With triethylamine; In dichloromethane; below 0 deg C;

DOI:10.1021/ja00317a060

Reference yield:

C9H10ClNO4S (88730-34-1) → Methanesulfonic acid 2-acetylamino-4-chloro-phenyl ester + Methanesulfonic acid 2-acetylamino-6-chloro-phenyl ester

Guidance literature:

In chloroform-d1; at 25 ℃; Rate constant; thermal rearrangement;

DOI:10.1021/ja00317a060

upstream raw materials:

N-(3-chlorophenyl)-N-hydroxyacetamide

methanesulfonyl chloride

N-(3-chlorophenyl)hydroxylamine

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