Reacción #344036
ord-c086264cb3754d7dbd62c47068519986
Ecuación de reacción
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1OtroIt was isolated by chromatography over 40 fold amount of silica gel
- 2OtroThe combined clean fractions were crystallized from hexane
- 3Otrorecrystallized from petroleum ether
- 4Otroto give colorless crystals with m.p. 127°-128°
Procedimiento
rac-3,4-dihydro-2,5,7,8-tetramethyl-2-[(1-naphthyl)ethynyl]-2H-1-benzopyran-6-ol was prepared by coupling rac-3,4-dihydro-2-ethynyl-2,5,7,8-tetramethyl-2H-1-benzopyran-6-ol with 1-iodonaphthalene under the conditions described in Example 1. It was isolated by chromatography over 40 fold amount of silica gel using methylene chloride. The combined clean fractions were crystallized from hexane and recrystallized from petroleum ether to give colorless crystals with m.p. 127°-128°.