Reacción #42386

ord-9aaf626347dc44ce96bbc4c487c5589d

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ConcentraciónThe reaction is then concentrated under reduced pressure
  2. 2
    workup.DISSOLUTIONredissolved in methylene chloride
  3. 3
    Lavadowashed with saturated sodium bicarbonate, water, and brine
  4. 4
    SecadoThe organic layer is then dried (sodium sulfate)
  5. 5
    Filtraciónfiltered
  6. 6
    Concentraciónconcentrated under reduced pressure

Procedimiento

To a solution of methyl 5-(bromomethyl)thiophene-2-carboxylate (350 mg, 1.49 mmol) in dry acetone (6.0 mL) is added N-methylbutylamine (533 μL, 4.47 mmol) and the solution stirred at room temperature overnight. The reaction is then concentrated under reduced pressure, redissolved in methylene chloride, washed with saturated sodium bicarbonate, water, and brine. The organic layer is then dried (sodium sulfate), filtered, and concentrated under reduced pressure to yield the title compound in pure form. 1H NMR (300 MHz, CDCl3) δ 7.65 (d, J=3 Hz, 1H), 6.88 (d, J=3 Hz, 1H), 3.86 (s, 3H), 3.69 (s, 2H), 2.41-2.36 (m, 2H), 2.25 (s, 3H), 1.53-1.43 (m, 2H), 1.34-1.25 (m, 2H), 0.91 (t, J=7 Hz, 3H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07727997B2uspto-grants-2010_06