2-acetamido-N-methyl-N-phenylbenzamide

Base Information

Chemical Name:2-acetamido-N-methyl-N-phenylbenzamide
CAS No.:94459-51-5
Molecular Formula:C₁₆H₁₆N₂O₂
Molecular Weight:268.315
Hs Code.:

Synonyms:2-acetamido-N-methyl-N-phenylbenzamide

Suppliers and Price of 2-acetamido-N-methyl-N-phenylbenzamide

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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-methyl-N-phenylbenzamide

Chemical Property:

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Technology Process of 2-acetamido-N-methyl-N-phenylbenzamide

There total 3 articles about 2-acetamido-N-methyl-N-phenylbenzamide 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: 85.0%

: 6632-37-7
2-amino-N-methyl-N-phenylbenzamide

: 75-36-5
acetyl chloride

: 94459-51-5
2-acetamido-N-methyl-N-phenylbenzamide

Guidance literature:: With pyridine; In dichloromethane; at 0 ℃;
DOI:10.1002/anie.201402925

Reference yield:

: 21563-73-5
2-aminobenzoyl chloride

: 94459-51-5
2-acetamido-N-methyl-N-phenylbenzamide

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dichloromethane / 0 - 20 °C

2: pyridine / dichloromethane / 0 °C

With pyridine; triethylamine; In dichloromethane;
DOI:10.1002/anie.201402925

Reference yield:

: 118-92-3,159201-01-1,50816-84-7,80206-34-4,104809-47-4
anthranilic acid

: 94459-51-5
2-acetamido-N-methyl-N-phenylbenzamide

Guidance literature:: Multi-step reaction with 3 steps

1: thionyl chloride / dichloromethane / 5 h / 20 °C

2: triethylamine / dichloromethane / 0 - 20 °C

3: pyridine / dichloromethane / 0 °C

With pyridine; thionyl chloride; triethylamine; In dichloromethane;
DOI:10.1002/anie.201402925