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4-aminophenol as a reactant in a 'Nucleophilic Acylation' reaction - page 1

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  1. acetyl bromide and 4-aminophenol react to form N-(4-hydroxyphenyl)acetamide
    CC(=O)Br.C1=CC(=CC=C1N)O>>CC(=O)NC1=CC=C(C=C1)O
  2. acetyl chloride and 4-aminophenol react to form N-(4-hydroxyphenyl)acetamide
    CC(=O)Cl.C1=CC(=CC=C1N)O>>CC(=O)NC1=CC=C(C=C1)O
  3. acetyl fluoride and 4-aminophenol react to form N-(4-hydroxyphenyl)acetamide
    CC(=O)F.C1=CC(=CC=C1N)O>>CC(=O)NC1=CC=C(C=C1)O
  4. acetyl iodide and 4-aminophenol react to form N-(4-hydroxyphenyl)acetamide
    CC(=O)I.C1=CC(=CC=C1N)O>>CC(=O)NC1=CC=C(C=C1)O
  5. 2-methylprop-2-enoyl bromide and 4-aminophenol react to form N-(4-hydroxyphenyl)-2-methyl-prop-2-enamide
    CC(=C)C(=O)Br.C1=CC(=CC=C1N)O>>CC(=C)C(=O)NC1=CC=C(C=C1)O
  6. 2-methylprop-2-enoyl chloride and 4-aminophenol react to form N-(4-hydroxyphenyl)-2-methyl-prop-2-enamide
    CC(=C)C(=O)Cl.C1=CC(=CC=C1N)O>>CC(=C)C(=O)NC1=CC=C(C=C1)O
  7. 2-methylprop-2-enoyl fluoride and 4-aminophenol react to form N-(4-hydroxyphenyl)-2-methyl-prop-2-enamide
    CC(=C)C(=O)F.C1=CC(=CC=C1N)O>>CC(=C)C(=O)NC1=CC=C(C=C1)O
  8. 2-methylprop-2-enoyl iodide and 4-aminophenol react to form N-(4-hydroxyphenyl)-2-methyl-prop-2-enamide
    CC(=C)C(=O)I.C1=CC(=CC=C1N)O>>CC(=C)C(=O)NC1=CC=C(C=C1)O
  9. N-methylcarbamoyl bromide and 4-aminophenol react to form (4-aminophenyl) N-methylcarbamate
    CNC(=O)Br.C1=CC(=CC=C1N)O>>CNC(=O)OC1=CC=C(C=C1)N
  10. N-methylcarbamoyl chloride and 4-aminophenol react to form (4-aminophenyl) N-methylcarbamate
    CNC(=O)Cl.C1=CC(=CC=C1N)O>>CNC(=O)OC1=CC=C(C=C1)N
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