Reaction #1483

ord-46f36199a03b442ba91746cd3e3add7b

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Otherwas periodically removed by a Dean-Stark trap
  2. 2
    OtherThe solvent was removed
  3. 3
    Otherthe residue was purified by column chromatography (silica, ethyl acetate/hexane (1/3))

Procedure

A solution of (±)6-(2-methyl-1,3-dioxolan-2-yl)-1,2,3,4-tetrahydro-4,4-dimethyl-1-hydroxy-1-(carboethoxymethyl)-naphthlene ((Compound D16, 321 mg, 0.90 mmol) and catalytic amount of TsOH in 20 ml of benzene was refluxed for 12 h. During the reaction the water generated from the reaction was periodically removed by a Dean-Stark trap. The solvent was removed and the residue was purified by column chromatography (silica, ethyl acetate/hexane (1/3)) to give the title compound as an oil (215 mg).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05723666uspto-grants-1998_03