Reaktion #628676

ord-244d5ca2497840e2aaff3b01be37a859

Reaktionsgleichung

[Al+3].[H-].[H-].[H-].[H-].[Li+]
lithium aluminum hydride
COC(=O)c1ccc2cc(Br)ccc2c1
Methyl 6-bromo-2-naphthoate
OCc1ccc2cc(Br)ccc2c1
(6-bromonaphthalen-2-yl)methanol
Ausbeute 75.4%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturTo a three-necked flask (5 L) cooled with an ice-bath
  2. 2
    workup.ADDITIONwas added dropwise slowly through a dropping funnel
  3. 3
    TemperaturCooling bath
  4. 4
    Sonstigewas removed
  5. 5
    TemperaturThe reaction mixture was cooled with an ice-bath again
  6. 6
    workup.ADDITIONto it was added methanol (150 mL) dropwise carefully until there
  7. 7
    workup.STIRRINGunder stirring for half an hour
  8. 8
    SonstigeThe resulting solid was removed
  9. 9
    Filtrationby filtering under reduced pressure
  10. 10
    Einengenthe filtrate was concentrated
  11. 11
    workup.ADDITIONpoured into deionized water (2 L)
  12. 12
    SonstigeThe resulting precipitate was collected by suction
  13. 13
    Filtrationfilter
  14. 14
    Waschenwashed with deionized water
  15. 15
    Sonstigedried in vacuum

Vorschrift

To a three-necked flask (5 L) cooled with an ice-bath was added lithium aluminum hydride (40 g, 1.05 mol), and anhydrous THF (500 mL) under nitrogen protection. To this suspension, Methyl 6-bromo-2-naphthoate (141 g, 0.534 mol) dissolved in anhydrous THF (1200 mL) was added dropwise slowly through a dropping funnel. Cooling bath was removed and the reaction mixture was kept under stirring for additional 2 hours. The reaction mixture was cooled with an ice-bath again, and to it was added methanol (150 mL) dropwise carefully until there was no gas release. The mixture was kept under stirring for half an hour and then was acidified with concentrated hydrochloric acid to a PH of about 4. The resulting solid was removed by filtering under reduced pressure and the filtrate was concentrated, and then poured into deionized water (2 L). The resulting precipitate was collected by suction filter, and washed with deionized water, followed by a little ethanol, and dried in vacuum to afford (6-bromonaphthalen-2-yl)methanol (95.4 g).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08872422B2uspto-grants-2014_10