Sandmeyer reaction
Aniline to halide
The Sandmeyer reaction is a chemical process that converts aromatic diazonium salts into aryl halides, cyanides, or other functional groups using copper catalysts.
It's a standard method in organic synthesis for introducing chlorine, bromine, or cyano groups onto a benzene ring: The Sandmeyer reaction allowed us to replace the amine with a chloride.
Amino-benzene compound
- benzene ringSix-membered carbon cycle
- nitrogen gasInert atmospheric element
- chlorinationDisinfecting with a halogen
- brominationAdding bromine to molecules
industrial chemistry · pharmaceuticals · agrochemicals · transition metal · catalyst
Amino-benzene compound
- nitrogen gasInert atmospheric element
- benzene ringSix-membered carbon cycle
aniline
Amino-benzene compound
- benzene ringSix-membered carbon cycle
- nitrogen gasInert atmospheric element
- chlorinationDisinfecting with a halogen
bromination · industrial chemistry · pharmaceuticals · agrochemicals · transition metal · catalyst
aniline
Amino-benzene compound
- nitrogen gasInert atmospheric element
- benzene ringSix-membered carbon cycle
aniline
Amino-benzene compound
- chemical reactionscondensation, combustion, oxidation, hydrolysis, oxidation-reduction
- Named ReactionsClaisen condensation, Negishi coupling, Sonogashira coupling
- Substitution ReactionsSN1, SN2, Friedel-Crafts, nitration, sulfonation
- diazo chemistry
- fluorination
- Halogenationbromination, chlorination, fluorination
reaction, reactionary, reactions, reactive, reactivity, overreaction, reactant, reactants, reactance