Acetamide, N-(4-methoxyphenyl)-N-(phenylmethyl)-

Base Information

• Chemical Name: Acetamide, N-(4-methoxyphenyl)-N-(phenylmethyl)-
• CAS No.: 61667-90-1
• Molecular Formula: C16H17NO2
• Molecular Weight: 255.316
• DSSTox Substance ID: DTXSID80487491
• Nikkaji Number: J2.126.170J
• Wikidata: Q82329528

Synonyms:61667-90-1;Acetamide, N-(4-methoxyphenyl)-N-(phenylmethyl)-;SCHEMBL10922368;DTXSID80487491

Chemical Property of Acetamide, N-(4-methoxyphenyl)-N-(phenylmethyl)-

Chemical Property:

• XLogP3: 2.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 255.125928785
• Heavy Atom Count: 19
• Complexity: 279

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=C(C=C2)OC

Technology Process of Acetamide, N-(4-methoxyphenyl)-N-(phenylmethyl)-

There total 3 articles about Acetamide, N-(4-methoxyphenyl)-N-(phenylmethyl)- 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: 99.0%

benzyl(4-methoxyphenyl)amine (17377-95-6) + acetyl chloride (75-36-5) → N-benzyl-N-(4-methoxyphenyl)acetamide (61667-90-1)

Guidance literature:

With triethylamine; In dichloromethane; at 20 ℃; for 1h;

DOI:10.1016/j.tet.2004.09.113

Reference yield: 68.0%

carbon monoxide (201230-82-2) + [4-(benzylideneamino)phenyl]methanol (783-08-4) + methyl iodide (74-88-4) → N-benzyl-N-(4-methoxyphenyl)acetamide (61667-90-1) + N-(4-Methoxy-phenyl)-N-(2-oxo-1-phenyl-propyl)-acetamide (120343-10-4)

Guidance literature:

With potassium hydroxide; PEG-400; dicobalt octacarbonyl; In dichloromethane; at 60 ℃; for 11h; under 760 Torr;

DOI:10.1016/S0040-4039(00)80693-0

Reference yield: 30.6%

acetic anhydride (108-24-7) + [4-(benzylideneamino)phenyl]methanol (783-08-4) → N-benzyl-N-(4-methoxyphenyl)acetamide (61667-90-1)

Guidance literature:

With diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate; In dichloromethane; for 6h; or with acetyl chloride;

upstream raw materials:

acetic anhydride

[4-(benzylideneamino)phenyl]methanol

carbon monoxide

methyl iodide

Downstream raw materials:

N-benzyl-2-{1-[chloro(p-tolylsulfinyl)methyl]cyclopentadecyl}-N-(4-methoxyphenyl)acetamide

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