Reacción #2254206

ord-05b7927134d14d40929b9583e3e9a32d

Ecuación de reacción

CC1(C)CC(=O)CCO1
tetrahydro-2,2-dimethyl-4H-pyran-4-one
[Li][CH2]CCC
n-BuLi
Cc1ccc(Br)cc1
4-bromo-toluene
Cc1ccc(C2(O)CCOC(C)(C)C2)cc1
2,2-dimethyl-4-(4-methylphenyl)oxan-4-ol

Disolventes

Condiciones de reacción

Temperatura
-78°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.STIRRINGThe resulting mixture was stirred at −78° C. for another 20 min
  2. 2
    Otroquenched
  3. 3
    workup.ADDITIONby adding MeOH (10 ml)
  4. 4
    ConcentraciónThe reaction was concentrated under vacuum
  5. 5
    workup.ADDITIONthe resulting residue was diluted with EtOAc (500 ml)
  6. 6
    Lavadowashed with sat. NH4Cl (250 ml), brine (250 ml)
  7. 7
    Otrodried
  8. 8
    Concentraciónconcentrated

Procedimiento

n-BuLi (26.3 ml, 1.6 M in hexane, 42 mmol) was added dropwise to a solution of 4-bromo-toluene (7.70 g, 45 mmol) in THF (100 ml) at −78° C. under N2. The resulting mixture was stirred at −78° C. for 30 min and a solution of tetrahydro-2,2-dimethyl-4H-pyran-4-one (3.84 g, 30 mmol) in THF (20 ml) was added. The resulting mixture was stirred at −78° C. for another 20 min and quenched by adding MeOH (10 ml). The reaction was concentrated under vacuum and the resulting residue was diluted with EtOAc (500 ml) and washed with sat. NH4Cl (250 ml), brine (250 ml), dried and concentrated to give 2,2-dimethyl-4-(4-methylphenyl)oxan-4-ol as a white solid, which was used without further purification (5.41 g, 82%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09044469B2uspto-grants-2015_06