Reaktion #2049472

ord-7336608d597a4903a122e69afda6f93c

Reaktionsgleichung

COC(=O)c1ccc2cc(Br)ccc2c1
methyl 6-bromo-2-naphthoate
C1CCOC1
THF
O.[Li+].[OH-]
lithium hydroxide hydrate
O=C(O)c1ccc2cc(Br)ccc2c1
title compound
O=C(O)c1ccc2cc(Br)ccc2c1
6-bromo-2-naphthoic acid

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    EinengenConcentrated under vacuum
  2. 2
    workup.ADDITIONdiluted with water
  3. 3
    Temperaturcooled to 0° C
  4. 4
    FiltrationSolids were collected by filtration
  5. 5
    workup.DISSOLUTIONdissolved in toluene-EtOAc (ca. 2 L)
  6. 6
    Waschenwashed with brine
  7. 7
    TrocknenDried over Na2SO4
  8. 8
    Filtrationfiltered
  9. 9
    Einengenconcentrated under vacuum
  10. 10
    SonstigeBrown solid was triturated with ether
  11. 11
    Filtrationcollected by filtration
  12. 12
    Sonstigedried under vacuum

Vorschrift

A solution of methyl 6-bromo-2-naphthoate (7.70 g, 29.0 mmol) in 2:1 THF:water (150 mL) was treated with lithium hydroxide hydrate (2.44 g, 58.1 mmol) followed by stirring at room temperature for 48 h. Concentrated under vacuum, diluted with water and cooled to 0° C. Acidified to pH3 with 4N HCl. Solids were collected by filtration, dissolved in toluene-EtOAc (ca. 2 L) and washed with brine. Dried over Na2SO4, filtered and concentrated under vacuum. Brown solid was triturated with ether, collected by filtration, and dried under vacuum to give the title compound as a nearly white solid (5.07 g, 70%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08415351B2uspto-grants-2013_04