Methanol → Methyl 8-aminooctanoate

HRID 324104

Reaktionsgleichung

Reaktionsgleichung von HRID 324104
S(Cl)(Cl)=O.[NH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][C:13]([OH:15])=[O:14].[CH3:16]O>>[NH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][C:13]([O:15][CH3:16])=[O:14]

Komponenten

4

Reaktionsbedingungen

Temperatur
-5 °C

Versuchsvorschrift

To 15 ml methanol under nitrogen, stirred, at −5° C. was added thionyl chloride (0.80 ml) dropwise. After 5 minutes, 8-aminooctanoic acid (1.592 g, 10 mmol) was added. The reaction was stirred at −5° C. for 1 h, room temperature for 45 minutes, and 40° C. for 2.25 h. After heating, the reaction mixture was concentrated. The residue was taken up in chloroform/water (40 ml/25 ml) and basified to pH 9-10 using 1N NaOH. Layers were shaken, separated and the aqueous layer washed with water (2×30 ml). The combined organics were dried over Na2SO4 and filtered. The filtrate was concentrated in vac and dried to give the product as an oily solid (1.568 g, 90%); 1H NMR (400 MHz, DMSO-d6) δ1.17-1.33 (m, 8H), 1.43-1.52 (m, 2H), 2.26 (t, J=7.5Hz, 2H), 2.44-2.49 (m, 2H), 3.55 (s, 3H); IR (film) 3475, 2930, 2850, 1730 cm−1; mass spectrum [EI], m/z 173 M+.

Aufarbeitung

  1. wait40° C. for 2.25 h
  2. temperatureAfter heating
  3. concentrationthe reaction mixture was concentrated
  4. stirringLayers were shaken
  5. customseparated
  6. washthe aqueous layer washed with water (2×30 ml)
  7. dry with materialThe combined organics were dried over Na2SO4
  8. filtrationfiltered
  9. concentrationThe filtrate was concentrated in vac
  10. customdried

Quellen und Nachweise

ORD-Eintrag
ord-eeb85ccec7c0406db7e3b835050ebb0a
Quelldatensatz
uspto-grants-2001_04
Patentnummer
US06214877B1

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