Reacción #1493

ord-e3e7b7ca98e641d6a2d408b95787c8d2

Ecuación de reacción

COC(=O)c1ccc2c(c1)C(Sc1ccccc1)=CCC2(C)C
methyl 5,5-dimethyl-5,6-dihydro-8-(phenylthio)-naphthalene-2-carboxylate
COC(=O)c1ccc2c(c1)C(Sc1ccccc1)=CCC2(C)C
Compound E18
COC(=O)c1ccc2c(c1)C(Sc1ccccc1)=CCC2(C)C
methyl 5,5-dimethyl-5,6-dihydro-8-(phenylthio)-naphthalene-2-carboxylate
[Na+].[OH-]
NaOH
CC1(C)CC=C(Sc2ccccc2)c2cc(C(=O)O)ccc21
title compound
CC1(C)CC=C(Sc2ccccc2)c2cc(C(=O)O)ccc21
5,5-Dimethyl-5,6-dihydro-8-(phenylthio)-naphthalene-2-carboxylic acid

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrowas quenched by the addition of 10% aqueous HCl
  2. 2
    ExtracciónThe mixture was extracted with EtOAc
  3. 3
    Lavadothe combined organic layers washed with H2O and saturated aqueous NaCl
  4. 4
    Secadobefore being dried over Na2SO4
  5. 5
    OtroRemoval of the solvents under pressure

Procedimiento

To a solution of methyl 5,5-dimethyl-5,6-dihydro-8-(phenylthio)-naphthalene-2-carboxylate (Compound E18, 300.0 mg, 0.926 mmol) in 4.0 mL of EtOH and 2.0 mL THF was added NaOH (200.0 mg, 5.00 mmol; 5.0 mL of a 1N aqueous solution). After stirring overnight at room temperature the reaction was quenched by the addition of 10% aqueous HCl. The mixture was extracted with EtOAc and the combined organic layers washed with H2O and saturated aqueous NaCl before being dried over Na2SO4. Removal of the solvents under pressure afforded the title compound as a yellow solid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05723666uspto-grants-1998_03