Reacción #66599

ord-c88dcfe861064e25825c480cf99cee92

Ecuación de reacción

O=C=O
dry ice
COc1cc(C=O)c(C(C)Cc2ccccc2)cc1OC
4,5-dimethoxy-2-(1-methyl-2-phenyl-ethyl)-benzaldehyde
CC1(C)CCCC(C)(C)N1
2,2,6,6-tetramethyl piperidine
[Li][CH2]CCC
n-Butyllithium
COc1ccnc(OC)n1
2,4-Dimethoxypyrimidine
COc1ncc(C(O)c2cc(OC)c(OC)cc2C(C)Cc2ccccc2)c(OC)n1
[4,5-dimethoxy-2-(1-methyl-2-phenyl-ethyl)-phenyl]-(2,4-dimethoxy-pyrimidin-5-yl)-methanol
Rendimiento 52.0%

Disolventes

Condiciones de reacción

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

Tratamiento posterior

  1. 1
    workup.ADDITIONwas added drop-wise over 5 minutes
  2. 2
    workup.STIRRINGAfter stirring for 1 hour the solution
  3. 3
    Temperaturawas warmed to room temperature
  4. 4
    Otroquenched by the slow addition of 50 mL 10% NH4Cl
  5. 5
    workup.ADDITIONAfter 100 mL of H2O was added the mixture
  6. 6
    Extracciónwas extracted with ethyl acetate
  7. 7
    Lavadowashed with H2O
  8. 8
    Lavadowashed with brine
  9. 9
    SecadoThe combined organics were dried over Na2SO4
  10. 10
    Filtraciónfiltered
  11. 11
    Concentraciónconcentrated in vacuo
  12. 12
    Otroto give an orange oil
  13. 13
    OtroPurification via flash chromatography (3:2 hexane/ethyl acetate)

Procedimiento

Freshly distilled 2,2,6,6-tetramethyl piperidine (0.85 mL, 5.0 mmol) was dissolved in 20 mL THF and cooled to 0° C. n-Butyllithium (2.0 mL, 2.5 M in hexanes) was added drop-wise over 5 minutes and the mixture was allowed to stir for 30 minutes and then cooled to −78° C. 2,4-Dimethoxypyrimidine (0.353 g, 2.52 mmol) was added drop-wise over 5 min. After 45 min the solution was transferred via a dry ice cooled cannula to a solution of 4,5-dimethoxy-2-(1-methyl-2-phenyl-ethyl)-benzaldehyde (0.717 g, 2.52 mmol) in 20 mL THF at −78° C. After stirring for 1 hour the solution was warmed to room temperature and quenched by the slow addition of 50 mL 10% NH4Cl. After 100 mL of H2O was added the mixture was extracted with ethyl acetate, washed with H2O and washed with brine. The combined organics were dried over Na2SO4, filtered and concentrated in vacuo to give an orange oil. Purification via flash chromatography (3:2 hexane/ethyl acetate) afforded [4,5-dimethoxy-2-(1-methyl-2-phenyl-ethyl)-phenyl]-(2,4-dimethoxy-pyrimidin-5-yl)-methanol (0.551 g, 52%) as a clear oil.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08524725B2uspto-grants-2013_09