Реакция #1489

ord-efe92404a0254b2b89ad1b766a802326

Уравнение реакции

CCOC(C)=O
EtOAc
CC1(C)CC=C(c2cccs2)c2cc(C(=O)O)ccc21
5,5-dimethyl-5,6-dihydro-8-(2-thienyl)-naphthalene-2-carboxylic acid
CC1(C)CC=C(c2cccs2)c2cc(C(=O)O)ccc21
Compound E6
CC1(C)CC=C(c2cccs2)c2cc(C(=O)O)ccc21
5,5-dimethyl-5,6-dihydro-8-(2-thienyl)-naphthalene-2-carboxylic acid
CCOC(=O)c1ccc(O)cc1
ethyl 4-hydroxybenzoate
CCN=C=NCCCN(C)C.Cl
1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride
CCOC(=O)c1ccc(OC(=O)c2ccc3c(c2)C(c2cccs2)=CCC3(C)C)cc1
title compound
CCOC(=O)c1ccc(OC(=O)c2ccc3c(c2)C(c2cccs2)=CCC3(C)C)cc1
Ethyl 4-[[(5,5-dimethyl-5,6-dihydro-8-(2-thienyl)-naphthalen-2-yl)carbonyl]oxy]-benzoate

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Промывкаthe solution washed with H2O, 5% HCl, saturated aqueous NaCO3, and saturated aqueous NaCl
  2. 2
    Сушкаbefore being dried over MgSO4
  3. 3
    ДругоеRemoval of the sovents under reduced pressure and column chromatography (10% EtOAc-hexanes) of the residual oil

Методика

A solution of 5,5-dimethyl-5,6-dihydro-8-(2-thienyl)-naphthalene-2-carboxylic acid (Compound E6, 50.0 mg, 0.177 mmol), ethyl 4-hydroxybenzoate (38.2 mg, 0.230 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (44.0 mg, 0.230 mmol), and 4-N,N-dimethylaminopyridine (28.0 mg, 0.230 mmol) in 2.0 mL DMF was stirred overnight at room temperature. EtOAc (50 mL) was added and the solution washed with H2O, 5% HCl, saturated aqueous NaCO3, and saturated aqueous NaCl before being dried over MgSO4. Removal of the sovents under reduced pressure and column chromatography (10% EtOAc-hexanes) of the residual oil afforded the title compound as a colorless solid.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05723666uspto-grants-1998_03