Reacción #1186198

ord-46764ac44eeb423e97af8d2be89458ee

Reactivos

Ninguno

Condiciones de reacción

Temperatura
45°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe title compound was synthesized
  2. 2
    FiltraciónThe reaction mixture was then filtered
  3. 3
    Lavadothe solid was washed with methylene chloride
  4. 4
    LavadoThe filtrate was washed three times with 50 ml of equal parts solution
  5. 5
    LavadoThe organic layer was washed with water and brine
  6. 6
    Secadodried over MgSO4
  7. 7
    Concentraciónconcentrated under reduced pressure

Procedimiento

The title compound was synthesized according to a literature method (Whitman Tetrahedron 1985, 41, 1183). To a mixture of 2-phenylacrylic acid methyl ester (7.92 g, 45 mmol) in 60 ml of methylene chloride was added mCPBA (13.1 g, 58.5 mmol) and the reaction was stirred at 45° C. overnight. The reaction mixture was then filtered and the solid was washed with methylene chloride. The filtrate was washed three times with 50 ml of equal parts solution consisting of saturated Na2S2O3 and saturated NaHCO3. The organic layer was washed with water and brine, dried over MgSO4, and concentrated under reduced pressure to afford the title compound in greater than 95% purity according to 1H NMR (85% yield). 1H NMR (CDCl3, 300 MHz) δ: 7.50-7.30 (m, 5H), 4.22 (q, J=7.2 Hz, 2H), 3.40 (d, J,=7.1 Hz, 1H), 2.95 (d, J=7.1 Hz, 1H), 1.26 (t, J=7.2 Hz, 3H) ppm.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08143375B2uspto-grants-2012_03