Réaction #45332

ord-871adde5e70a454ab25b5529dd7b5246

Solvants

Conditions de réaction

Température
60°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    ExtractionThe resultant mixture was extracted with EtOAc (100 mL)
  2. 2
    Lavagethe organic layer was washed with brine (50 mL)
  3. 3
    Séchagedried over Na2SO4
  4. 4
    Filtrationfiltered
  5. 5
    Concentrationconcentrated
  6. 6
    AutrePurification by flash chromatography with 50% EtOAc/hexanes

Mode opératoire

To a solution of 3-nitro-5-(trifluoromethyl)benzoic acid (2.0 g, 8.5 mmol) in THF (100 mL) was added borane-THF (17 mL of a 1 M solution in THF, 17 mmol). The reaction was stirred at 60° C. for 24 hours and then poured into H2O (50 mL). The resultant mixture was extracted with EtOAc (100 mL) and the organic layer was washed with brine (50 mL), dried over Na2SO4, filtered, and concentrated. Purification by flash chromatography with 50% EtOAc/hexanes afforded [3-nitro-5-(trifluoromethyl)phenyl]methanol. Rf=0.35 (75% EtOAc/hexanes). 1H NMR (CDCl3, 500 MHz) 8.44 (s, 1H), 8.40 (s, 1H), 7.98 (s, 1H), 4.91 (s, 2H), 2.07 (bs, 1H).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07737295B2uspto-grants-2010_06