Reaction #363440

ord-6e68bfb8a2134a28b6bf190ddde2c6b9

Solvents

Conditions

Temperature
20°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Temperaturecooled to 4° C
  2. 2
    Otherto quench
  3. 3
    Otherthe reaction
  4. 4
    workup.DISSOLUTIONto dissolve the resulting solids
  5. 5
    ExtractionThe resulting solution was extracted with Et2O (200 mL)
  6. 6
    DryingThe organic layer was dried (Na2SO4)
  7. 7
    Concentrationconcentrated under reduced pressure

Procedure

To a solution of LiAlH4 (0.93 g, 24.4 mmol) and AlCl3 (3.24 g, 24.4 mmol) in THF at 4° C. was added dropwise a solution of 14-aza-7-oxadispiro[4.2.5.1]tetradecane (2.38 g, 12,2 mmol) in THF (15 mL). The resulting mixture was warmed to 20° C. and stirred for 45 min., then cooled to 4° C. Water (5 mL) was slowly added to quench the reaction and a 1N NaOH solution (85 mL) was added to dissolve the resulting solids. The resulting solution was extracted with Et2O (200 mL). The organic layer was dried (Na2SO4) and concentrated under reduced pressure to yield 1-(cyclohexylamino)-1-(hydroxymethyl)cyclopentane 1.89 g (79%): GC-MS m/z 197 (M+).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06353006B1uspto-grants-2002_03