N-Bromosuccinimide: Difference between revisions
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File:NBS_Bromohydrin_Formation_Scheme_(cropped).png|Bromohydrin formation using N-Bromosuccinimide | |||
File:NBS_Fluorination.png|Fluorination reaction with N-Bromosuccinimide | |||
File:NBS_allylic_bromination_scheme.svg|Allylic bromination using N-Bromosuccinimide | |||
File:NBS_Alpha-Bromination_Scheme_(cropped).png|Alpha-bromination with N-Bromosuccinimide | |||
File:Hoffmann_Rearrangement_NBS.png|Hoffmann rearrangement with N-Bromosuccinimide | |||
File:NBS_Oxidation_Corey.png|Oxidation reaction by Corey using N-Bromosuccinimide | |||
File:Decarboxylation_of_alpha-amino_acid_with_NBS.svg|Decarboxylation of alpha-amino acid with N-Bromosuccinimide | |||
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Latest revision as of 11:32, 18 February 2025
N-Bromosuccinimide or NBS is a chemical compound with the formula C4H4BrNO2. It is a white crystalline solid that is often used in organic chemistry for bromination reactions.
Structure and Properties[edit]
N-Bromosuccinimide is a brominated derivative of succinimide. It has a planar, cyclic structure with a bromine atom attached to the nitrogen atom. The molecule is polar due to the presence of the bromine atom, which is highly electronegative. This makes NBS soluble in polar solvents such as water and alcohol.
Synthesis[edit]
N-Bromosuccinimide is typically synthesized from succinimide and bromine in the presence of water. The reaction proceeds via a nucleophilic substitution mechanism, with the bromine atom replacing one of the hydrogen atoms on the nitrogen atom of the succinimide.
Uses[edit]
N-Bromosuccinimide is widely used in organic chemistry as a brominating agent. It is particularly useful for selective bromination reactions, where it can be used to selectively brominate a specific position in a molecule. This is due to its ability to generate low concentrations of bromine in situ, which can react with specific sites in a molecule.
Safety[edit]
N-Bromosuccinimide is a strong oxidizer and can react violently with reducing agents. It is also corrosive and can cause burns to skin and eyes. Proper safety precautions should be taken when handling this compound.
See Also[edit]
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Bromohydrin formation using N-Bromosuccinimide
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Fluorination reaction with N-Bromosuccinimide
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Allylic bromination using N-Bromosuccinimide
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Alpha-bromination with N-Bromosuccinimide
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Hoffmann rearrangement with N-Bromosuccinimide
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Oxidation reaction by Corey using N-Bromosuccinimide
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Decarboxylation of alpha-amino acid with N-Bromosuccinimide

