Hydrochloric Acid → 4-Hydrazinophenyl propionamide hydrochloride

HRID 1683258Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1683258
[ClH:1].[NH2:2][C:3]1[CH:8]=[CH:7][C:6]([CH:9]([CH3:13])[C:10]([NH2:12])=[O:11])=[CH:5][CH:4]=1.[N:14]([O-])=O.[Na+]>O>[ClH:1].[NH:2]([C:3]1[CH:4]=[CH:5][C:6]([CH:9]([CH3:13])[C:10]([NH2:12])=[O:11])=[CH:7][CH:8]=1)[NH2:14]

Komponenten

5

Edukt 3

HCID 313Hydrochloric Acid2×HCID 128052284-Aminophenyl propionamideHCID 23668193Sodium Nitrite

Produkt 1

HCID 189442744-Hydrazinophenyl propionamide hydrochloride

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

Concentrated hydrochloric acid (4 ml) was added slowly, with cooling and stirring to 4-aminophenyl propionamide (0.80 g), maintaining the temperature below 5° C. To this slurry was added a solution of sodium nitrite (0.37 g) in water (2 ml), dropwise over 15 min, followed by stirring for a further 15 min. The turbid solution thus formed was added portionwise to a cooled, stirred solution of stannous chloride (2.19 g) in conclusion. HCl (4 ml), and the resulting mixture was stirred for 1 h. After filtering, the solution was reduced in volume until an inorganic precipitate formed. This was filtered off, and the filtrate was evaporated to dryness. The residual gum was crystallized from acetic acid to give crude 4-hydrazinophenyl propionamide hydrochloride (1.05 g).

Aufarbeitung

  1. temperaturewith cooling
  2. temperaturemaintaining the temperature below 5° C
  3. customThe turbid solution thus formed
  4. additionwas added portionwise to a cooled
  5. filtrationAfter filtering
  6. customformed
  7. filtrationThis was filtered off
  8. customthe filtrate was evaporated to dryness
  9. customThe residual gum was crystallized from acetic acid

Quellen und Nachweise

ORD-Eintrag
ord-8ee988cc107e4ea38bc2182aadf6cbf9
Quelldatensatz
uspto-grants-1997_06
Patentnummer
US05637611

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