Reaktion #698223

ord-e38aa1522d3944bdb5246e13125143d0

Reaktionsgleichung

COC(=O)c1ccc2c(c1)C(c1cccs1)=CCC2(C)C
methyl 5,5-dimethyl-5,6-dihydro-8-(2-thienyl)-2-naphthalenecarboxylate
COC(=O)c1ccc2c(c1)C(c1cccs1)=CCC2(C)C
Compound E5
COC(=O)c1ccc2c(c1)C(c1cccs1)=CCC2(C)C
methyl 5,5-dimethyl-5,6-dihydro-8-(2-thienyl)-2-naphthalenecarboxylate
[Na+].[OH-]
NaOH
CC1(C)CC=C(c2cccs2)c2cc(C(=O)O)ccc21
title compound
CC1(C)CC=C(c2cccs2)c2cc(C(=O)O)ccc21
5,5-dimethyl-5,6-dihydro-8-(2-thienyl)-naphthalene-2-carboxylic acid

Lösungsmittel

Reaktionsbedingungen

Temperatur
35°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturcooled to room temperature
  2. 2
    Sonstigequenched with 1M HCl
  3. 3
    ExtraktionThe mixture was extracted with EtOAc
  4. 4
    Waschenthe combined organic layers washed with H2O and saturated aqueous NaCl
  5. 5
    Trocknenbefore being dried over MgSO4
  6. 6
    SonstigeRemoval of the solvents under reduced pressure

Vorschrift

To a solution of methyl 5,5-dimethyl-5,6-dihydro-8-(2-thienyl)-2-naphthalenecarboxylate (Compound E5, 430.0 mg, 1.44 mmol) in 3.0 mL of EtOH and 3.0 mL THF was added NaOH (240.0 mg, 6.00 mmol; 3.0 mL of a 2N aqueous solution). The resulting solution was warmed to 35° C. for 6 h, cooled to room temperature and quenched with 1M HCl. The mixture was extracted with EtOAc and the combined organic layers washed with H2O and saturated aqueous NaCl before being dried over MgSO4. Removal of the solvents under reduced pressure afforded the title compound as a pale yellow solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05998655uspto-grants-1999_12