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  1. Problemas de prática
  2. Orgânica 2
  3. Síntese e transformação de aminas
  4. Reductive amination — acetone and methylamine

Química Orgânica 2 · Síntese e transformação de aminas

Reductive amination — acetone and methylamine

Desenhe o mecanismo · Desafio

Condições: Acetone and methylamine condense with a water-mediated proton relay, then hydronium is added. A separate formal reduction of the isolated iminium ion follows. Only one B–H transfer from BH₄⁻ is shown, not a proposed one-pot reaction: ordinary borohydride is not generally stable or iminium-selective in strongly acidic solution. The waters show where the oxygen and hydrogen atoms end up, not a complete reduction medium. Stop before borane association or quench; counterions are omitted spectators. No asymmetric induction is assumed.

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Arraste dos elétrons que se movem até onde eles vão, ou toque em um e depois no outro. Cada seta é verificada; Dica ajuda quando você travar. Não precisa de conta.

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← Todos os problemas de Síntese e transformação de aminasPróximo problema: Hofmann rearrangement — N-bromoamide to a shorter amine →

O mecanismo, passo a passo

Próximo mostra as setas curvas de cada passo e as explica. Os passos escritos estão abaixo.

Ler todos os 6 passos escritos
  1. Carbonyl and nitrogen encounter

    The amine lone pair supplies the new C–N bond. The carbonyl pair moves to oxygen.

    As setas curvas

    • The amine lone pair supplies the new C–N bond.
    • The carbonyl pair moves to oxygen.
  2. Solvent-mediated proton exchange

    Water accepts an N-bound proton as part of the coupled relay. The N–H pair restores the nitrogen lone pair. Alkoxide accepts a water proton in the same relay. The departing O–H pair replenishes the solvent oxygen lone pair. Water mediates a coupled relay. No isolated hydronium/alkoxide pair or direct unassisted N-to-O proton transfer is implied.

    Nota: Water mediates a coupled relay. No isolated hydronium/alkoxide pair or direct unassisted N-to-O proton transfer is implied.

    As setas curvas

    • Water accepts an N-bound proton as part of the coupled relay.
    • The N–H pair restores the nitrogen lone pair.
    • Alkoxide accepts a water proton in the same relay.
    • The departing O–H pair replenishes the solvent oxygen lone pair.
  3. Acid stage

    The hydroxy oxygen accepts a hydronium proton. Hydronium returns to neutral water. Hydronium is added here. Its spectator counteranion is omitted throughout.

    Nota: Hydronium is added here. Its spectator counteranion is omitted throughout.

    As setas curvas

    • The hydroxy oxygen accepts a hydronium proton.
    • Hydronium returns to neutral water.
  4. Continue the condensation branch

    Nitrogen donates its pair to form the C=N bond. The C–O pair departs onto the oxygen of neutral water.

    As setas curvas

    • Nitrogen donates its pair to form the C=N bond.
    • The C–O pair departs onto the oxygen of neutral water.
  5. Formal reduction of the isolated iminium ion

    The B–H pair makes a carbon–hydrogen bond at electrophilic iminium carbon; no free hydride is released. The iminium pi pair returns to nitrogen as carbon gains hydrogen, preserving both octets and giving a neutral amine. Condensation has ended. BH₄⁻ is added only for this separate formal reduction of the isolated iminium ion. This does not imply BH₄⁻ stability or selective one-pot reduction in acid. Waters remain to show the fate of their atoms. Borane association and quench are not shown.

    Nota: This is a separate formal reduction, not an acidic one-pot borohydride reaction. Waters remain to show the fate of their atoms; the drawing does not specify which borane species exist in solution.

    As setas curvas

    • The B–H pair makes a carbon–hydrogen bond at electrophilic iminium carbon; no free hydride is released.
    • The iminium pi pair returns to nitrogen as carbon gains hydrogen, preserving both octets and giving a neutral amine.
  6. Secondary amine at the transfer endpoint

    The carbonyl carbon now bears nitrogen and the transferred hydride. The original oxygen remains in water with a solvent proton and the acid proton, while the solvent shuttle retains the original N proton. Nitrogen has three sigma bonds and a lone pair; BH₄⁻ becomes the formally neutral BH₃ fragment. Every atom from the added reagents is retained.

O que você vai praticar

Join carbinolamine formation and dehydration to a formal isolated-iminium hydride transfer, retaining carbonyl oxygen in water.

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Tags

  • #ReductiveAmination
  • #IminesAndEnamines
  • #Amines
  • #MechanismDrawing

Mais problemas de Síntese e transformação de aminas

  • Hofmann rearrangement — N-bromoamide to a shorter amine
  • Gabriel synthesis — phthalimide alkylation and deprotection
  • Hinsberg reaction — secondary-amine sulfonylation
  • A nitrogen–nitrogen bond from a secondary amine
  • Two nitrogen origins in an aryl diazonium ion
  • Fischer indole synthesis: follow the two nitrogens
  • Reduce an amide all the way to an amine
  • Trimethylamine N-oxide

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  • Síntese e transformação de aminas: problemas de prática
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