Reaktion #45332

ord-871adde5e70a454ab25b5529dd7b5246

Reaktionsgleichung

O
H2O
O=C(O)c1cc([N+](=O)[O-])cc(C(F)(F)F)c1
3-nitro-5-(trifluoromethyl)benzoic acid
B.C1CCOC1
borane THF
O=[N+]([O-])c1cc(CO)cc(C(F)(F)F)c1
[3-nitro-5-(trifluoromethyl)phenyl]methanol

Lösungsmittel

Reaktionsbedingungen

Temperatur
60°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    ExtraktionThe resultant mixture was extracted with EtOAc (100 mL)
  2. 2
    Waschenthe organic layer was washed with brine (50 mL)
  3. 3
    Trocknendried over Na2SO4
  4. 4
    Filtrationfiltered
  5. 5
    Einengenconcentrated
  6. 6
    SonstigePurification by flash chromatography with 50% EtOAc/hexanes

Vorschrift

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).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07737295B2uspto-grants-2010_06