Reacción #1647

ord-32e98db4036848ce8b8264c0ec0c3131

Ecuación de reacción

CCOC(C)=O
ethyl acetate
Cc1cn(COCOC(=O)c2ccccc2)c(=O)[nH]c1=O
1-[(benzoyloxy)methoxymethyl]thymine
CCC(CC)OP(=O)(O)O
diethyl phosphonomethanol
C[Si](C)(C)OS(=O)(=O)C(F)(F)F
trimethylsilyl trifluoromethanesulfonate
CCOP(=O)(COCOCn1cc(C)c(=O)[nH]c1=O)OCC
title compound
CCOP(=O)(COCOCn1cc(C)c(=O)[nH]c1=O)OCC
1-[(Diethylphosphonomethoxy)methoxymethyl]thymine

Disolventes

Condiciones de reacción

Temperatura
85°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaAfter cooling to room temperature
  2. 2
    Lavadowashed with aqueous bicarbonate, brine
  3. 3
    Secadodried (MgSO4)
  4. 4
    Filtraciónfiltered
  5. 5
    Concentraciónconcentrated in vacuo
  6. 6
    OtroThe resultant yellow oil was purified by silica gel column chromatography

Procedimiento

To a solution of 1-[(benzoyloxy)methoxymethyl]thymine (2.9 g, 10 mmol) and diethyl phosphonomethanol (1.85 g, 11 mmol) in benzene (180 mL) was added trimethylsilyl trifluoromethanesulfonate (0.05 mL) via a syringe under nitrogen. The solution was heated at 85° C. for 20 min. After cooling to room temperature, ethyl acetate (50 mL) was added and washed with aqueous bicarbonate, brine dried (MgSO4), filtered and concentrated in vacuo. The resultant yellow oil was purified by silica gel column chromatography using CH2Cl2 /5% MeOH as an eluent to give the title compound as a white oil: yield 980 mg (30%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05726174uspto-grants-1998_03