Potassium borohydride → 3-Aminononan-2-ol

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°.

1. temperaturecooled to -10° in an ice-salt bath
2. additionwas added in small portions over a 2-3 hr
3. customto reach room temperature
4. custom(22°)
5. customThe mixture is then evaporated to dryness (syrup) in vacuo
6. custompartitioned between H2O (150 ml) and chloroform (150 ml)
7. extractionThe H2O layer was further extracted (3×) with chloroform (100 ml ea.)
8. dry with materialThe chloroform layer was dried with MgSO4
9. customevaporated in vacuo
10. customto give a slightly yellowish, oily product
11. distillationThis liquid was distilled in high vacuo at 95°-100° (0.15 mm Hg)

ORD record

ord-59639191eb424664b25d837175247a6c

Source dataset

uspto-grants-1980_09

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US04221909