Stannous Chloride → Ethyl 2-chloro-5-hydrazinocinnamate

HRID 984781Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 984781
[Sn](Cl)Cl.[NH2:4][C:5]1[CH:6]=[CH:7][C:8]([Cl:18])=[C:9]([CH:17]=1)[CH:10]=[CH:11][C:12]([O:14][CH2:15][CH3:16])=[O:13].[N:19]([O-])=O.[Na+]>Cl>[Cl:18][C:8]1[CH:7]=[CH:6][C:5]([NH:4][NH2:19])=[CH:17][C:9]=1[CH:10]=[CH:11][C:12]([O:14][CH2:15][CH3:16])=[O:13]

Komponenten

5

Edukt 3

HCID 24479Stannous ChlorideHCID 23668193Sodium NitriteHCID 54425193Ethyl 5-amino-2-chlorocinnamate

Produkt 1

HCID 54155293Ethyl 2-chloro-5-hydrazinocinnamateAusbeute 34,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 313Hydrochloric AcidLösungsmittel

Versuchsvorschrift

First. 60 g of tin (11) chloride was dissolved in 60 ml of concentrated hydrochloric acid, and the mixture was cooled to −30° C., to which a diazonium solution prepared from 19 g of ethyl 5-amino-2-chlorocinnamate and 6.3 g of sodium nitrite was added dropwise at 0° C. or lower. The reaction mixture was stirred at room temperature for 1 hour, and the precipitated crystals were collected by filtration. These crystals were added to ice-water, neutralized with 2N aqueous sodium hydroxide, and extracted with chloroform. The chloroform layer was dried and concentrated, which afforded 7.0 g of ethyl 2-chloro-5-hydrazinocinnamate.

Aufarbeitung

  1. additionwas added dropwise at 0° C.
  2. filtrationthe precipitated crystals were collected by filtration
  3. additionThese crystals were added to ice-water
  4. extractionextracted with chloroform
  5. dry with materialThe chloroform layer was dried
  6. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-779f2a65a89b4a9198ae62e5b6c57b50
Quelldatensatz
uspto-grants-2005_03
Patentnummer
US06869913B1

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