Reaktion #40266

ord-8195caeae8504cdfb40a16fc4ca39ca5

Reaktionsgleichung

O=C1CCC(=O)N1Cl
N-chlorosuccinimide
Oc1ccc2cc(Br)ccc2c1
6-bromo-2-naphthol
Oc1ccc2cc(Br)ccc2c1Cl
6-bromo-1-chloro-2-naphthol
Ausbeute 95.4%

Lösungsmittel

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe synthesis of (S1-2)
  2. 2
    TemperaturThe reaction solution was heated to room temperature
  3. 3
    Waschenwashed with saturated sodium bicarbonate solution and water
  4. 4
    Trocknendried over magnesium sulfate
  5. 5
    workup.DISTILLATIONdistilled under a reduced pressure
  6. 6
    Sonstigeto remove the solvent
  7. 7
    SonstigeRecrystallization

Vorschrift

The synthesis of (S1-2) was carried out following the method described in Synlett, No. 18, 2837 (2005), wherein 29.9 g of N-chlorosuccinimide and 600 ml of dichloromethane were added to a reactor in nitrogen atmosphere and cooled to 0° C., 2.6 g of zirconium (IV) chloride was added, and then 50 g of 6-bromo-2-naphthol (S1-1) was added slowly. The reaction solution was heated to room temperature and stirred for 10 hours, then washed with saturated sodium bicarbonate solution and water, dried over magnesium sulfate, and distilled under a reduced pressure to remove the solvent. Recrystallization was carried out using a mixed solvent of toluene/heptane=1/1 (volumetric ratio) to obtain 55 g of 6-bromo-1-chloro-2-naphthol (S1-2).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07727417B2uspto-grants-2010_06