반응 #55868

ord-59639191eb424664b25d837175247a6c

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도cooled to -10° in an ice-salt bath
  2. 2
    workup.ADDITIONwas added in small portions over a 2-3 hr
  3. 3
    기타to reach room temperature
  4. 4
    기타(22°)
  5. 5
    기타The mixture is then evaporated to dryness (syrup) in vacuo
  6. 6
    기타partitioned between H2O (150 ml) and chloroform (150 ml)
  7. 7
    추출The H2O layer was further extracted (3×) with chloroform (100 ml ea.)
  8. 8
    건조The chloroform layer was dried with MgSO4
  9. 9
    기타evaporated in vacuo
  10. 10
    기타to give a slightly yellowish, oily product
  11. 11
    workup.DISTILLATIONThis liquid was distilled in high vacuo at 95°-100° (0.15 mm Hg)

실험 절차

3-Amino-2-nonanol hydrochloride (43.8 g, 0.226 mole) was dissolved in absolute methanol (150 ml) and cooled to -10° in an ice-salt bath. 1. Potassium borohydride (24.4 g, 0.45 mole) 2. was added in small portions over a 2-3 hr. period. The mixture is then kept at -10° to -15° for 3 hr. 3,4. and slowly allowed to reach room temperature (22°), then stirred overnight (20 hr.) at room temperature. The mixture is then evaporated to dryness (syrup) in vacuo and partitioned between H2O (150 ml) and chloroform (150 ml). The H2O layer was further extracted (3×) with chloroform (100 ml ea.). The chloroform layer was dried with MgSO4 and evaporated in vacuo to give a slightly yellowish, oily product. This liquid was distilled in high vacuo at 95°-100° (0.15 mm Hg) to give pure erythro- 3-amino-2-nonanol, 26.4 g, 75% yield, m.p. 81°-86°.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04221909uspto-grants-1980_09