Reaktion #1476

ord-1def6f145a124de08c583f52bfc46d3d

Reaktionsgleichung

CC(C)OB(OC(C)C)OC(C)C
triisopropylborate
CC1(C)CCCc2cc(Br)ccc21
6-bromo-1,2,3,4-tetrahydro-1,1-dimethylnaphthalene
[Li][CH2]CCC
n-BuLi
CC1(C)CCCc2cc(B(O)O)ccc21
title compound
CC1(C)CCCc2cc(B(O)O)ccc21
(5,6,7,8-Tetrahydro-5,5-dimethylnaphth-2-yl)boronic acid

Lösungsmittel

Reaktionsbedingungen

Temperatur
-78°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGthe reaction stirred at room temperature for 12 h
  2. 2
    Extraktionextracted with ether (2×)
  3. 3
    WaschenThe combined organic layer was washed with brine
  4. 4
    Trocknendried over MgSO4
  5. 5
    Einengenconcentrated in vacuo
  6. 6
    Sonstigeto give an oil
  7. 7
    SonstigeRecrystallization from hexane

Vorschrift

To a cold (-78° C.) solution of 2.02 g (8.4 mmol) of 6-bromo-1,2,3,4-tetrahydro-1,1-dimethylnaphthalene in 11.0 mL of toluene, was added 4.6 g (6.8 mL, 10.9 mmol, 1.6M in hexane) of n-BuLi. The resulting solution was stirred at -78° C. for 45 min. and then 2.40 g (3.0 mL, 12.7 mmol) of triisopropylborate was dropwise added and the reaction stirred at room temperature for 12 h. The reaction was then diluted with 10% HCl, and extracted with ether (2×). The combined organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo to give an oil. Recrystallization from hexane afforded the title compound as a white solid.

Quelle

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