Reaktion #74384

ord-461ada4e5d714353aa4cb3f14f78972c

Reaktionsgleichung

OO
H2O2
[Na+].[OH-]
NaOH
O=C1C[C@H]2C[C@@H]1CC2(F)F
(1R,4R)-5,5-difluorobicyclo[2.2.1]heptan-2-one
CCC(C)[BH-](C(C)CC)C(C)CC.[Li+]
L-Selectride
O[C@@H]1C[C@H]2C[C@@H]1CC2(F)F
title compound
O[C@@H]1C[C@H]2C[C@@H]1CC2(F)F
(1R,2R,4R)-5,5-Difluorobicyclo[2.2.1]heptan-2-ol

Lösungsmittel

Reaktionsbedingungen

Temperatur
-78°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe mixture was warmed to r.t.
  2. 2
    workup.STIRRINGstirred at 65° C. for 10 h
  3. 3
    TemperaturAfter cooling to ambient temperature
  4. 4
    Extraktionthe mixture was extracted with EtOAc (50 mL×2)
  5. 5
    WaschenThe combined organic portions were washed with brine

Vorschrift

To a solution of (1R,4R)-5,5-difluorobicyclo[2.2.1]heptan-2-one (0.540 g, 3.7 mmol) in anhydrous tetrahydrofuran (8.00 mL) at −78° C. under nitrogen was added drop-wise L-Selectride (1.0 M solution in tetrahydrofuran, 7.40 mL). After stirring at −78° C. for 3 h, 30% H2O2 (6.0 mL) and 10% NaOH (aq., 10.0 mL) were added. The mixture was warmed to r.t. and then stirred at 65° C. for 10 h. After cooling to ambient temperature, the mixture was extracted with EtOAc (50 mL×2). The combined organic portions were washed with brine, and conc. in vacuo. Flash column chromatography (0 to 30% of ethyl acetate in hexanes) gave the title compound as a white solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08541592B2uspto-grants-2013_09