Reaktion #52236

ord-69907c3ae526490195aad8c034f65fdb

Reaktionsgleichung

CC(C)(C)OC(=O)N1CCC(C(=O)O)CC1
1-Boc-isonipecotic acid
B.C1CCOC1
BH3-THF
CC(C)(C)OC(=O)N1CCC(CO)CC1
l-Boc-piperidine-4-methanol
Ausbeute 85.0%

Reagenzien

Keine

Lösungsmittel

Reaktionsbedingungen

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

Aufarbeitung

  1. 1
    Temperaturto warm to room temperature for 12 h
  2. 2
    SonstigeThe mixture was carefully quenched with water
  3. 3
    workup.ADDITIONdiluted with ethyl acetate
  4. 4
    ExtraktionThe water layer was extracted with ethyl acetate
  5. 5
    Waschenwashed with brine
  6. 6
    Trocknendried (Na2SO4)
  7. 7
    Filtrationfiltered
  8. 8
    Einengenconcentrated

Vorschrift

1-Boc-isonipecotic acid (10.0 g, 214 mmol) was dissolved in THF (400 mL) and cooled to 0° C. A solution of BH3-THF (180 mL, 1 N in THF, 180 mmol) was added slowly. The mixture stirred for 1 h at 0° C. and was allowed to warm to room temperature for 12 h. The mixture was carefully quenched with water and diluted with ethyl acetate. The water layer was extracted with ethyl acetate. The organic layers were combined, washed with brine, dried (Na2SO4), filtered and concentrated to provide l-Boc-piperidine-4-methanol (7.98 g, 85%) as a white solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06855715B1uspto-grants-2005_02