Reacción #43905

ord-0fc48cb907c544e4a4e86b869454a751

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturacooling
  2. 2
    workup.STIRRINGthe mixture was stirred at room temperature for 1 hr
  3. 3
    FiltraciónThe insoluble substance was filtered off through celite
  4. 4
    Concentraciónthe filtrate was concentrated under reduced pressure

Procedimiento

To a solution of methyl 4′-[(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)oxy]-2′,6′-dimethylbiphenyl-3-carboxylate (0.128 g, 0.33 mmol) in tetrahydrofuran (2 mL) was added lithium aluminum hydride (80%, 15.7 mg, 0.33 mmol) by small portions under ice-cooling, and the mixture was stirred at the same temperature for 1.5 hr. Sodium sulfate 10 hydrate (0.106 g, 0.33 mmol) was added by small portions to the reaction mixture, and the mixture was stirred at room temperature for 1 hr. The insoluble substance was filtered off through celite, and the filtrate was concentrated under reduced pressure to give the title compound (0.111 g, yield 93%) as a colorless amorphous powder.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07732626B2uspto-grants-2010_06