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4-aminophenol as a reactant in a 'Nucleophilic Acylation' reaction - page 2

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