Reaktion #1472

ord-97b20453788c4bc8828b820164729c18

Reaktionsgleichung

CCOC(C)=O
ethyl acetate
CCOC(=O)c1ccc2cc(Br)ccc2c1
ethyl 6-bromo-naphthalene-2-carboxylate
Cc1ccccc1
toluene
CC1(C)CCCc2cc(B(O)O)ccc21
(5,6,7,8-tetrahydro-5,5-dimethylnaphth-2-yl)boronic acid
CCOC(=O)c1ccc2cc(C3Cc4ccccc4C(C)(C)C3)ccc2c1
title compound
CCOC(=O)c1ccc2cc(C3Cc4ccccc4C(C)(C)C3)ccc2c1
Ethyl-6-[5,6,7,8-tetrahydro-5,5-dimethyl-naphth-7-yl]naphth-2-oate

Reaktionsbedingungen

Temperatur
80°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionextracted with CH2Cl2 (2×)
  2. 2
    Waschenthe organic layer was washed with brine
  3. 3
    Trocknendried over MgSO4
  4. 4
    Einengenconcentrated in vacuo
  5. 5
    Sonstigeto give an oil

Vorschrift

To a degassed solution of 0.39 g (1.4 mmol) of ethyl 6-bromo-naphthalene-2-carboxylate and 3.0 mL of toluene, was added sequentially 49 mg (0.04 mmol) of tetrakis-triphenylphosphine palladium(0), 2.0 mL (2.0 mmol) of 1M sodium carbonate and then a solution of 0.32 g (1.6 mmol) of (5,6,7,8-tetrahydro-5,5-dimethylnaphth-2-yl)boronic acid (Compound B13) in 3.0 mL of MeOH. The reaction was heated at 80° C. for 6 h, diluted with 2N Na2CO3, and extracted with CH2Cl2 (2×), the organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo to give an oil. Flash chromatography (silica, 5% ethyl acetate in hexane) of the crude material gave the title compound as a white solid.

Quelle

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