Реакция #1483

ord-46f36199a03b442ba91746cd3e3add7b

Уравнение реакции

CCOC(=O)CC1(O)CCC(C)(C)c2cc(C3(C)OCCO3)ccc21
(±)6-(2-methyl-1,3-dioxolan-2-yl)-1,2,3,4-tetrahydro-4,4-dimethyl-1-hydroxy-1-(carboethoxymethyl)-naphthlene
Cc1ccc(S(=O)(=O)O)cc1
TsOH
O
water
CCOC(=O)CC1=CCC(C)(C)c2cc(C(C)=O)ccc21
title compound
CCOC(=O)CC1=CCC(C)(C)c2cc(C(C)=O)ccc21
3,4-Dihydro-4,4-dimethyl-1-(carboethoxymethyl)-6-acetyl-naphthalene

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

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

Методика

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).

Источник

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