Hydrochloric Acid → 2-Acetylamino-6-methyl-6-nitroheptanoic acid

HRID 1744021Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1744021
[C:1]([NH:4][C:5]([CH2:16][CH2:17][CH2:18][C:19]([CH3:24])([N+:21]([O-:23])=[O:22])[CH3:20])(C(OCC)=O)[C:6]([O:8]CC)=[O:7])(=[O:3])[CH3:2].[OH-].[K+].Cl>C(O)C.O>[C:1]([NH:4][CH:5]([CH2:16][CH2:17][CH2:18][C:19]([CH3:24])([N+:21]([O-:23])=[O:22])[CH3:20])[C:6]([OH:8])=[O:7])(=[O:3])[CH3:2]

Komponenten

6

Reaktionsbedingungen

Temperatur
90 °C

Versuchsvorschrift

Diethyl 2-acetylamino-2-(4-methyl-4-nitropentyl)malonate (193.5 g, 558.5 mmol) was dissolved in ethanol (270 ml), and potassium hydroxide (51 g, 781.9 mmol) was dissolved in water (250 ml) and added. The mixture was stirred at 90° C. for 1 h, and potassium hydroxide (51 g, 781.9 mmol) was dissolved in water (250 ml) and added. The mixture was stirred at the same temperature for 2 h. The mixture was cooled to 40° C. and concentrated hydrochloric acid was added to adjust the solution to pH 1.5, which solution was stirred overnight at 80° C. Ethanol was evaporated by concentration under reduced pressure and the residue was ice-cooled. The precipitated crystals were separated, and the obtained slurry was washed with ethyl acetate (200 ml) and dried under reduced pressure to give the objective compound (99.6 g, yield 72%).

Aufarbeitung

  1. additionadded
  2. additionadded
  3. stirringThe mixture was stirred at the same temperature for 2 h
  4. temperatureThe mixture was cooled to 40° C.
  5. stirringwas stirred overnight at 80° C
  6. customEthanol was evaporated by concentration under reduced pressure
  7. temperaturecooled
  8. customThe precipitated crystals were separated
  9. washthe obtained slurry was washed with ethyl acetate (200 ml)
  10. customdried under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-65b6724ca9034f3c87783c0012a80ae2
Quelldatensatz
uspto-grants-2006_03
Patentnummer
US07012152B2

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