N-(Benzenecarbothioyl)-N-(1-phenylethyl)acetamide

Base Information

• Chemical Name: N-(Benzenecarbothioyl)-N-(1-phenylethyl)acetamide
• CAS No.: 89873-89-2
• Molecular Formula: C17H17NOS
• Molecular Weight: 283.394
• DSSTox Substance ID: DTXSID20532833

Synonyms:89873-89-2;N-(Benzenecarbothioyl)-N-(1-phenylethyl)acetamide;DTXSID20532833

Chemical Property of N-(Benzenecarbothioyl)-N-(1-phenylethyl)acetamide

Chemical Property:

• XLogP3: 3.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 283.10308534
• Heavy Atom Count: 20
• Complexity: 343

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

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

Technology Process of N-(Benzenecarbothioyl)-N-(1-phenylethyl)acetamide

There total 1 articles about N-(Benzenecarbothioyl)-N-(1-phenylethyl)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: 100.0%

acetyl chloride (75-36-5) + N-[1-phenylethyl]benzenecarbothioamide (64551-86-6) → N-(1-Phenyl-ethyl)-N-thiobenzoyl-acetamide (89873-89-2)

Guidance literature:

DOI:10.1021/jo00184a037

Reference yield: 95.0%

N-(1-Phenyl-ethyl)-N-thiobenzoyl-acetamide (89873-89-2) → N-(1-Methyl-1,2-diphenyl-2-thioxo-ethyl)-acetamide (89873-95-0)

Guidance literature:

In benzene; Irradiation;

DOI:10.1021/jo00184a037

Reference yield:

N-(1-Phenyl-ethyl)-N-thiobenzoyl-acetamide (89873-89-2) + acetyl chloride (75-36-5) → Thioacetic acid S-(1-acetyl-3-methyl-2,3-diphenyl-aziridin-2-yl) ester (89874-01-1)

Guidance literature:

With triethylamine; Multistep reaction; 1.) hv, toluene, -78 deg C, 2.) -78 deg C;

DOI:10.1021/jo00184a037

upstream raw materials:

acetyl chloride

N-[1-phenylethyl]benzenecarbothioamide

Downstream raw materials:

N-(1-Methyl-1,2-diphenyl-2-thioxo-ethyl)-acetamide

Thioacetic acid S-(1-acetyl-3-methyl-2,3-diphenyl-aziridin-2-yl) ester

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