Reacción #344036

ord-c086264cb3754d7dbd62c47068519986

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroIt was isolated by chromatography over 40 fold amount of silica gel
  2. 2
    OtroThe combined clean fractions were crystallized from hexane
  3. 3
    Otrorecrystallized from petroleum ether
  4. 4
    Otroto 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°.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05260294uspto-grants-1993_11