Reacción #1771994

ord-4e7dee2502b84ab18ecf35021b18dcc9

Ecuación de reacción

CC1(C(=O)O)CCCCC1
1-methyl-1-hydroxycarbonylcyclohexane
B#B
diborane
CC1(CO)CCCCC1
1-methyl-1-hydroxymethylcyclohexane
Rendimiento 69.0%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe cooling bath was removed
  2. 2
    OtroThe remaining borane was quenched by the slow addition of saturated sodium bisulfate (10 mL) over 90 min
  3. 3
    Temperaturawith cooling
  4. 4
    workup.ADDITIONAdditional saturated sodium bisulfate (200 mL) was added and after 20 min
  5. 5
    workup.STIRRINGof stirring the aqueous layer
  6. 6
    Otrowas removed
  7. 7
    LavadoThe organic layer was washed with water and saturated sodium chloride
  8. 8
    Otrodried
  9. 9
    Filtraciónfiltered
  10. 10
    Concentraciónconcentrated
  11. 11
    OtroThe residue was purified by flash chromatography

Procedimiento

To a solution of 1-methyl-1-hydroxycarbonylcyclohexane (10 g, 70 mmol) in tetrahydrofuran(300 mL) at 0° C. was added 1M diborane in tetrahydrofuran (200 mL, 200 mmol) over 90 minutes. The cooling bath was removed and the reaction mixture was stirred at room temperature for two days. The remaining borane was quenched by the slow addition of saturated sodium bisulfate (10 mL) over 90 min with cooling. Additional saturated sodium bisulfate (200 mL) was added and after 20 min of stirring the aqueous layer was removed. The organic layer was washed with water and saturated sodium chloride, dried, filtered and concentrated. The residue was purified by flash chromatography using 20% diethylether in hexanes to give 1-methyl-1-hydroxymethylcyclohexane (6.17 g, 48 mmol, 69%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: USRE043298E1uspto-grants-2012_04