Reacción #1495908
ord-81f57eb9f139426a9aafbe5e4e1de3ee
Ecuación de reacción
Reactivos
Ninguno
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1TemperaturaThe suspension was refluxed overnight
- 2OtroThen the solvent was removed in vacuo
- 3workup.ADDITIONCH2Cl2 was added to the resulting residue and insoluble material
- 4Filtraciónfiltered off
- 5LavadoThe filtrate was washed with H2O
- 6Otrodried
- 7Concentraciónconcentrate in vacuo
- 8OtroThe crude product was purified by column chromatography
Procedimiento
To a solution of 6-bromo-2′,4′,5′,6′-tetrahydrospiro[chroman-2,3′-pyran]-4-one (2 g, 6.8 mmol) in MeOH Selectfluor™ (2.5 g, 7.1 mmol) was added. The suspension was refluxed overnight. Then the solvent was removed in vacuo. CH2Cl2 was added to the resulting residue and insoluble material filtered off. The filtrate was washed with H2O, dried and concentrate in vacuo. The crude product was purified by column chromatography to give 6-bromo-3-fluoro-2′,4′,5′,6′-tetrahydrospiro[chroman-2,3′-pyran]-4-one (220 mg, 10%). 1H-NMR (CDCl3): 1.72-2.21 (m, 4H), 3.44 (m, 1H), 3.63 (m, 1H), 3.73 (m, 1H), 3.92 (m, 1H), 4.91 (m, 1H), 6.94 (m, 1H), 7.56 (m, 1H), 7.90 (m, 1H).