Similiar Molecules

• SMILES String: C1=CC=C(C=C1)NC(=O)CCl
• Also know as: 2-chloro-N-phenyl-acetamide
• InChI=1/C8H8ClNO/c9-6-8(11)10-7-4-2-1-3-5-7/h1-5H,6H2,(H,10,11)/f/h10H
• Molecular Formula: C8H8ClNO
Reactions where this compound is a product:
• (Amide Formation from an Acid Chloride)
0
from 2-chloroacetyl chloride, aniline

• (Nucleophilic Acylation)
0
from 2-chloroacetyl bromide, aniline

• from 2-chloroacetyl chloride, aniline
  
• from 2-chloroacetyl fluoride, aniline
  
• from 2-chloroacetyl iodide, aniline
  
Reactions where this compound is a reactant:
• (Amide Formation from an Acid Chloride)
0
with acetyl chloride2-chloro-N-phenyl-aceta to form N-acetyl-2-chloro-N-phenyl-acetamide

• (Aldol Condensation)
0
with formic acid2-chloro-N-phenyl-aceta to form (Z)-2-chloro-3-hydroxy-N-phenyl-prop-2-enamide

• (Nucleophilic Acylation)
0
with acetyl bromide2-chloro-N-phenyl-aceta to form N-acetyl-2-chloro-N-phenyl-acetamide

• with acetyl chloride2-chloro-N-phenyl-aceta to form N-acetyl-2-chloro-N-phenyl-acetamide
  
• with acetyl fluoride2-chloro-N-phenyl-aceta to form N-acetyl-2-chloro-N-phenyl-acetamide
  
• with acetyl iodide2-chloro-N-phenyl-aceta to form N-acetyl-2-chloro-N-phenyl-acetamide
  
• (Sn2)
0
with 2-bromo-1-methoxy-propane2-chloro-N-phenyl-aceta to form 2-chloro-N-(2-methoxy-1-methyl-ethyl)-N-phenyl-acetamide

• with 2-chloro-1-methoxy-propane2-chloro-N-phenyl-aceta to form 2-chloro-N-(2-methoxy-1-methyl-ethyl)-N-phenyl-acetamide
  
• with 2-fluoro-1-methoxy-propane2-chloro-N-phenyl-aceta to form 2-chloro-N-(2-methoxy-1-methyl-ethyl)-N-phenyl-acetamide
  
• with 2-chloro-N-phenyl-acetamide to form N-phenyl-2-ureido-acetamide
  
• with 2-chloro-N-phenyl-acetamidecyclopropanecarboxylic to form [2-oxo-2-(phenylamino)ethyl] cyclopropanecarboxylate
  
• with 2-chloro-N-phenyl-acetamide(Z)-3-(2-furyl)prop-2-enoic to form [2-oxo-2-(phenylamino)ethyl] (E)-3-(2-furyl)prop-2-enoate
  
• with 2-chloro-N-phenyl-acetamideethyl (2E)-2-(4-oxothiazolidin-2-ylidene)ace to form ethyl (2Z)-2-[4-oxo-3-[2-oxo-2-(phenylamino)ethyl]thiazolidin-2-ylidene]acetate
  
• with 2-chloro-N-phenyl-acetamide1,3-diazaspiro[4.4]nonane-2,4-d to form 2-(2,4-dioxo-1,3-diazaspiro[4.4]nonan-3-yl)-N-phenyl-acetamide
  
• with 2-chloro-N-phenyl-acetamidecyclohexanecarboxylic to form [2-oxo-2-(phenylamino)ethyl] cyclohexanecarboxylate
  
• with 2-chloro-N-phenyl-acetamide(Z)-but-2-enoic to form [2-oxo-2-(phenylamino)ethyl] (E)-but-2-enoate
  
See all 68 reactions
• (Enolate Substitution)
0
with acetic acid2-chloro-N-phenyl-aceta to form 4-oxo-4-(phenylamino)butanoic acid

• with methyl acetate2-chloro-N-phenyl-aceta to form methyl 4-oxo-4-(phenylamino)butanoate
  
• with 2-chloro-N-phenyl-acetamidebromomet to form 2-chloro-N-phenyl-propanamide
  
• with 2-chloro-N-phenyl-acetamidechloromet to form 2-chloro-N-phenyl-propanamide
  
• with 2-chloro-N-phenyl-acetamideiodomet to form 2-chloro-N-phenyl-propanamide
  
• with 2-chloro-N-phenyl-acetamidebromoet to form 2-chloro-N-phenyl-butanamide
  
• with 2-chloro-N-phenyl-acetamidechloroet to form 2-chloro-N-phenyl-butanamide
  
• with 2-chloro-N-phenyl-acetamideiodoet to form 2-chloro-N-phenyl-butanamide
  
• with N-phenylacetamide2-chloro-N-phenyl-aceta to form N,N'-di(phenyl)butanediamide
  
• with propionic acid2-chloro-N-phenyl-aceta to form 2-methyl-4-oxo-4-(phenylamino)butanoic acid
  
See all 87 reactions
• (Friedel-Crafts acylation)
0
with 2-chloro-N-phenyl-acetamideacetyl chlo to form N-(3-acetylphenyl)-2-chloro-acetamide

• with 2-chloro-N-phenyl-acetamideacetyl chlo to form N-(4-acetylphenyl)-2-chloro-acetamide
  
• with 2-chloro-N-phenyl-acetamideacetyl chlo to form N-(2-acetylphenyl)-2-chloro-acetamide
  
• (Friedel-Crafts alkylation)
0
with 2-chloro-N-phenyl-acetamidechloromet to form 2-chloro-N-(4-methylphenyl)acetamide

• with 2-chloro-N-phenyl-acetamidechloromet to form 2-chloro-N-(2-methylphenyl)acetamide
  
• with 2-chloro-N-phenyl-acetamidechloromet to form 2-chloro-N-(3-methylphenyl)acetamide
  
• (Electrophilic aromatic bromination)
0
with 2-chloro-N-phenyl-ace to form N-(4-bromophenyl)-2-chloro-acetamide

• (Electrophilic aromatic iodination)
0
with 2-chloro-N-phenyl-ace to form 2-chloro-N-(4-iodophenyl)acetamide

• with 2-chloro-N-phenyl-ace to form 2-chloro-N-(3-iodophenyl)acetamide
  
• with 2-chloro-N-phenyl-ace to form 2-chloro-N-(2-iodophenyl)acetamide
  
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