Reacción #1178486
ord-d5c7517da7614fc0acfb8db975970eae
Ecuación de reacción
Reactantes
Reactivos
Ninguno
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1ConcentraciónThe reaction liquor was concentrated under reduced pressure
- 2Extracciónthe obtained residue was extracted with methylene chloride
- 3LavadoThe extract was washed with saturated brine
- 4Secadodried over anhydrous sodium sulfate
- 5ConcentraciónThe solvent was concentrated under reduced pressure
- 6Otrothe obtained residue was purified by thin layer chromatography (ethyl acetate
Procedimiento
To an aqueous solution (1 mL) of methyl N-benzyloxycarbonyl-2,5-dideoxy-3-O-ethyl-2,5-imino-D-lyxofuranoside, trifluoroacetic acid (1 mL) was added, and the mixture was stirred for three hours. The reaction liquor was concentrated under reduced pressure, and the obtained residue was extracted with methylene chloride. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was concentrated under reduced pressure, and the obtained residue was purified by thin layer chromatography (ethyl acetate:n-hexane=1:1, v/v), to obtain the title compound (92 mg, 77%) as an oily matter.