Hydrochloric Acid → HCID 178436837, Verbindung

HRID 1484476

Reaktionsgleichung

Reaktionsgleichung von HRID 1484476
[OH:1][NH:2][C:3]([NH2:5])=[O:4].CO.CO[CH:10](OC)[CH2:11][C:12](=O)[CH2:13][CH3:14].C(O)C.[ClH:21]>>[ClH:21].[CH2:13]([C:12]1[N:5]=[C:3]([OH:4])[N+:2]([O-:1])=[CH:10][CH:11]=1)[CH3:14]

Komponenten

6

Reaktionsbedingungen

Temperatur
-6.5 °C

Versuchsvorschrift

0.388 mol (25.9 g) hydroxy urea were dissolved in 195 ml 2 M HCl, 80 ml of methanol were added and 0.388 mol (56.7 g) of 1,1-dimethoxypentane-3-on (62% content in product mixture) were added dropwise under cooling with the internal temperature being maintained at −6 to −7° C. The solution was thawed to room temperature in an ice bath and stirred for 1 h, then evaporated until dryness. The residue was suspended with 100 ml of acetone, the mixture was cooled to below 0° C. in an ice/ethanol bath, the solid filtered off and washed with little ice-cold acetone. After drying 32.6 g crude product were obtained. The crude product was heated until boiling with 200 ml ethanol, hot filtered and slowly cooled to −18° C. The precipitated solid was filtered off, washed with a little amount of ethanol and dried. 11.7 g of the title compound were obtained.

Aufarbeitung

  1. temperatureunder cooling with the internal temperature
  2. customThe solution was thawed to room temperature in an ice bath
  3. customevaporated until dryness
  4. temperaturethe mixture was cooled to below 0° C. in an ice/ethanol bath
  5. filtrationthe solid filtered off
  6. washwashed with little ice-cold acetone
  7. dry with materialAfter drying 32.6 g crude product
  8. customwere obtained
  9. filtrationhot filtered
  10. temperatureslowly cooled to −18° C
  11. filtrationThe precipitated solid was filtered off
  12. washwashed with a little amount of ethanol
  13. customdried

Quellen und Nachweise

ORD-Eintrag
ord-dcb726fdc3bb4008bcf77046605c0b12
Quelldatensatz
uspto-grants-2016_08
Patentnummer
US09422247B2

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