Reaktion #88016

ord-579a58a9a073434b8d6c85cba9929bfe

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.WAITthe reaction was left
  2. 2
    Extraktionextracted with EtOAc (×3)
  3. 3
    Trocknenthe combined organic layers were dried over sodium sulfate
  4. 4
    Sonstigethe solvent was removed

Vorschrift

To a solution of ethyl 5-bromothiophene-2-carboxylate (1.5 g, 6.38 mmol) in aqueous conc. H2SO4 (6 ml) cooled to 0° C., aqueous 65% HNO3 (2 ml) was added, and the reaction was left to warm to RT and stirred for 1 hour. The mixture was poured into ice-water and extracted with EtOAc (×3); the combined organic layers were dried over sodium sulfate and the solvent was removed affording ethyl 5-bromo-4-nitrothiophene-2-carboxylate (Int. 40) which was used without any additional purification (550 mg, 1.964 mmol).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09440954B2uspto-grants-2016_09