Reaktion #1483

ord-46f36199a03b442ba91746cd3e3add7b

Reaktionsgleichung

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

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

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

Vorschrift

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).

Quelle

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