Reaktion #76083

ord-973796534d3b4bfcbae335a1b94886d0

Lösungsmittel

Reaktionsbedingungen

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

Aufarbeitung

  1. 1
    TemperaturThe mixture was cooled to 0° C.
  2. 2
    Temperaturwas heated to 80° C. for 45 minutes
  3. 3
    TemperaturThe mixture was cooled to room temperature
  4. 4
    Einengenconcentrated under reduced pressure to a white solid
  5. 5
    workup.ADDITIONtreated with 2 M NaOH in order
  6. 6
    ExtraktionThe basic solution was extracted with diethyl ether (3×)
  7. 7
    WaschenThe organic layers were washed with brine (2×)
  8. 8
    Trocknendried over anhydrous sodium sulfate
  9. 9
    Einengenconcentrated

Vorschrift

To a stirred solution of the mixture containing 1-(4-hydroxymethyl-phenyl)-cyclopropanecarboxylic acid heptylamide (Example 28, 1.0 g) in tetrahydrofuran (30 mL) under an nitrogen atmosphere cooled to 0° C. was added sodium borohydride (20.7 mmol, 783 mg) in one portion followed by the dropwise addition of boron trifluoride diethyletherate (27.6 mmol, 3.50 ml). The heterogeneous white mixture was allowed to stir at room temperature for 16 hours. The mixture was cooled to 0° C. and 2 M HCl was added until gas evolution ceased, then was heated to 80° C. for 45 minutes. The mixture was cooled to room temperature and concentrated under reduced pressure to a white solid. The solid was suspended in water (50 mL), then treated with 2 M NaOH in order to bring the pH to 14. The basic solution was extracted with diethyl ether (3×). The organic layers were washed with brine (2×), dried over anhydrous sodium sulfate, and concentrated to give impure [4-(1-heptylaminomethyl-cyclopropyl)-phenyl]-methanol as a clear oil. The crude oil was used in the preparation of heptyl-[1-(4-hydroxymethyl-phenyl)-cyclopropylmethyl]-carbamic acid tert-butyl ester without further purification.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06699904B2uspto-grants-2004_03