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Semicarbazide hydrochloride → 2-Chloro-5,6-dimethylnicotinaldehyde

HRID 903345
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 903345
[Cl:1][C:2]1[C:7]([C:8]#N)=[CH:6][C:5]([CH3:10])=[C:4]([CH3:11])[N:3]=1.Cl.NNC(N)=[O:16].C([O-])(=O)C.[Na+]>[Ni].O.CO>[Cl:1][C:2]1[C:7]([CH:8]=[O:16])=[CH:6][C:5]([CH3:10])=[C:4]([CH3:11])[N:3]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 3

HCID 11236Semicarbazide hydrochlorideHCID 517045Sodium AcetateHCID 128911062-Chloro-5,6-dimethylpyridine-3-carbonitrile

Produkt 1

HCID 127838462-Chloro-5,6-dimethylnicotinaldehydeAusbeute 60,5 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 935NickelKatalysator
HCID 887
Methanol
Lösungsmittel
HCID 962WaterLösungsmittel2×

Versuchsvorschrift

A mixture of 2-chloro-3-cyano-5,6-dimethylpyridine (21.5 g), semicarbazide hydrochloride (24.0 g), sodium acetate (42.3 g), water (225 ml) and methanol (475 ml) was hydrogenated at 344 kPa at 50° using Raney nickel catalyst (5 g). The mixture was added to water (750 ml) and filtered. The solid filtered off was suspended in water (130 ml) and concentrated hydrochloric acid (70 ml) was added and the mixture was heated at 100° for 1 hour; formalin (40% w/w, 120 ml) was added and the mixture was heated at 100° for a further 0.5 hour and allowed to cool. Sodium acetate (95 g) and water (250 ml) were added and the mixture was extracted with ether and the extracts were washed with 5% aqueous potassium carbonate and evaporated to give 2-chloro-5,6-dimethyl-3-pyridinecarboxaldehyde (13.24 g, 60%), m.p. 69°-70°.

Aufarbeitung

  1. customwas hydrogenated at 344 kPa at 50°
  2. filtrationfiltered
  3. filtrationThe solid filtered off
  4. additionconcentrated hydrochloric acid (70 ml) was added
  5. temperaturethe mixture was heated at 100° for 1 hour
  6. additionformalin (40% w/w, 120 ml) was added
  7. temperaturethe mixture was heated at 100° for a further 0.5 hour
  8. temperatureto cool
  9. additionSodium acetate (95 g) and water (250 ml) were added
  10. extractionthe mixture was extracted with ether
  11. washthe extracts were washed with 5% aqueous potassium carbonate
  12. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-46166b7d2f45434c8adf4c17f85e5881
Quelldatensatz
uspto-grants-1980_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04227000

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