Reaktion #1179

ord-70a25d6a367f495c9c26f59a04ae0cc2

Reaktionsgleichung

O=N[O-].[Na+]
NaNO2
[Cl][Sn][Cl]
SnCl2
Cc1c(N)ccc(C(=O)O)c1C
4-amino-2,3-dimethylbenzoic acid
Cc1c(NN)ccc(C(=O)O)c1C.Cl
expected product
Ausbeute 93.7%
Cc1c(NN)ccc(C(=O)O)c1C.Cl
2,3-Dimethyl-4-hydrazinobenzoic acid hydrochloride
Ausbeute 93.7%

Lösungsmittel

Reaktionsbedingungen

Temperatur
-5°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGthe mixture is stirred for 30 minutes at -5° C.
  2. 2
    Sonstige2 hours
  3. 3
    Sonstigeat RT
  4. 4
    FiltrationThe mixture is filtered
  5. 5
    Waschenthe precipitate is washed with 5 ml of concentrated HCl
  6. 6
    Sonstigedried under a stream of dry nitrogen

Vorschrift

A solution of 1.87 g of NaNO2 in 7 ml of water is added slowly to a solution, cooled to -5° C., of 4.5 g of 4-amino-2,3-dimethylbenzoic acid in 135 ml of concentrated HCl. After 2 hours of stirring at -5° C., a solution of 25 g of SnCl2 ·2H2O in 250 ml of concentrated HCl is added at -10° C., and the mixture is stirred for 30 minutes at -5° C. and then 2 hours at RT. The mixture is filtered, and the precipitate is washed with 5 ml of concentrated HCl and dried under a stream of dry nitrogen and then under vacuum to obtain 5.5 g of expected product.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05723483uspto-grants-1998_03