2-Hydrazinoethanol → 2-(5-Amino-3-methyl-1H-pyrazol-1-yl)ethan-1-ol

HRID 1250420Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1250420
[NH2:1]/[C:2](/[CH3:6])=[CH:3]\[C:4]#[N:5].[OH:7][CH2:8][CH2:9][NH:10]N>C(O)CCCC>[NH2:5][C:4]1[N:10]([CH2:9][CH2:8][OH:7])[N:1]=[C:2]([CH3:6])[CH:3]=1

Komponenten

4

Edukt 2

HCID 80172-HydrazinoethanolHCID 5325263(2Z)-3-Amino-2-butenenitrile

Produkt 1

HCID 50183732-(5-Amino-3-methyl-1H-pyrazol-1-yl)ethan-1-olAusbeute 63,8 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 62761-PentanolLösungsmittel

Versuchsvorschrift

To a solution of 16.4 g (0.2 mol) of 3-aminocrotononitrile in 100 cm3 of n-pentanol were added 16.7 g (0.22 mol) of β-hydroxyethylhydrazine and the mixture was then heated at reflux for 12 hours. The n-pentanol was subsequently distilled off under reduced pressure. A thick oil was obtained, which crystallizes by addition of 150 cm3 of isopropyl ether. A beige solid was obtained, which was filtered off on a sinter funnel. After drying under vacuum at 40° C., 18 g of the expected product were obtained in the form of a beige solid, the melting point of which was from 66 to 68° C.

Aufarbeitung

  1. temperaturethe mixture was then heated
  2. temperatureat reflux for 12 hours
  3. distillationThe n-pentanol was subsequently distilled off under reduced pressure
  4. customA thick oil was obtained
  5. customwhich crystallizes by addition of 150 cm3 of isopropyl ether
  6. customA beige solid was obtained
  7. filtrationwhich was filtered off on a sinter funnel
  8. customAfter drying under vacuum at 40° C.

Quellen und Nachweise

ORD-Eintrag
ord-2aae05c061134227a58cbf3f0c285490
Quelldatensatz
uspto-grants-2002_01
Patentnummer
US06338741B1

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