Reacción #364707

ord-711df7b430b147e4b0f7f92f153a5364

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe organic phase was separated
  2. 2
    Lavadowashed (water and brine)
  3. 3
    Secadodried (MgSO4)

Procedimiento

110 mg (0.31 mmol) of ethyl 4-[(5,6,7,8-tetrahydro-5-hydroxy-8,8-dimethylnaphth-2-yl)ethynyl]benzoate (Compound 9) in a mixture of THF and methanol was refluxed with 1 ml (1 mmol) of LiOH (1M aqueous solution). Thereafter the mixture was diluted with Et2O:EtOAc (1:1), and acidified with aqueous HCl to pH5. The organic phase was separated, washed (water and brine), dried (MgSO4) to yield the title compound.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06355806B1uspto-grants-2002_03