N-(4-amino-3-chlorophenyl)acetamide

Base Information

• Chemical Name: N-(4-amino-3-chlorophenyl)acetamide
• CAS No.: 16604-99-2
• Molecular Formula: C8H9ClN2O
• Molecular Weight: 184.62
• European Community (EC) Number: 899-532-1
• Nikkaji Number: J195.860G
• Mol file: 16604-99-2.mol

Synonyms:N-(4-amino-3-chlorophenyl)acetamide;16604-99-2;4/'-Amino-3/'-chloroacetanilide;4'-Amino-3'-chloroacetanilide;4-acetylamino-2-chloroaniline;SCHEMBL5459120;AKOS009494795;EN300-66903;G20862;Z425366400

Chemical Property of N-(4-amino-3-chlorophenyl)acetamide

Chemical Property:

• PSA: 55.12000
• LogP: 2.53480
• XLogP3: 1.5
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 184.0403406
• Heavy Atom Count: 12
• Complexity: 174

Purity/Quality:

N-(4-amino-3-chlorophenyl)acetamide ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(=O)NC1=CC(=C(C=C1)N)Cl

Technology Process of N-(4-amino-3-chlorophenyl)acetamide

There total 3 articles about N-(4-amino-3-chlorophenyl)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: 24.0%

3-chloro-4-nitroacetanilide (712-33-4) + methylhydrazine (60-34-4) → 4-amino-3-chloronitroacetanilide (16604-99-2) + 5-acetylamino-1-methyl-1H-benzotriazole (26947-54-6)

Guidance literature:

In ethanol; at 150 ℃; for 5h;

DOI:10.3987/COM-98-S(H)34

Reference yield:

3-chloro-4-nitroacetanilide (712-33-4) → 4-amino-3-chloronitroacetanilide (16604-99-2)

Guidance literature:

With iron; acetic acid;

Reference yield:

→ 4-amino-3-chloronitroacetanilide (16604-99-2)

Guidance literature:

With hydrogen; In methanol; at 80 ℃; for 2.5h; under 6000.6 Torr; Autoclave;

upstream raw materials:

3-chloro-4-nitroacetanilide

methylhydrazine

Downstream raw materials:

N-( 4-acetylamino-2-chlorophenyl)-5-chloro-2-hydroxybenzamide

Refernces

• 1、 Sanna, Paolo,Carta, Antonio,Paglietti, Giuseppe. "Synthesis of triazolo[4,5-f]quinolines. An unusual case of displacement of nitro group in the reaction of 8-acetylamino-6-chloro-5-nitroquinoline with hydrazine and methylhydrazine". . p. 693 - 702. Retrieved 2007/10/03.