Reaktion #88907

ord-d7dc88ac9347472191ed93b7249b1547

Reaktionsgleichung

Cc1ccc(N)cc1O
4-amino-2-hydroxytoluene
O=N[O-].[Na+]
sodium nitrite
[Cl][Sn][Cl]
tin (II) chloride
Cc1ccc(NN)cc1O.Cl
title compound
Ausbeute 127.1%
Cc1ccc(NN)cc1O.Cl
5-Hydrazino-2-methyl-phenol hydrochloride salt
Ausbeute 127.1%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe mixture was cooled in an ice/water bath
  2. 2
    Filtrationthe solid collected by filtration
  3. 3
    Waschenwashing with ice-cold cyclohexane
  4. 4
    SonstigeThe residue was dried in vacuo at 50° C.

Vorschrift

To an ice cold slurry of 4-amino-2-hydroxytoluene (6.22 g, 50.0 mmol), ice (10.0 g) and hydrochloric acid (37% aqueous, 15.0 mL) was added an ice-cold solution of sodium nitrite (3.49 g, 50.0 mmol) in water (10.0 mL) over 30 min. The resultant slurry was added over 30 min to an ice-cold slurry of tin (II) chloride (25.3 g, 133 mmol) in water (30.0 mL) and hydrochloric acid (37% aqueous, 30.0 mL) and the reaction stirred overnight. The mixture was cooled in an ice/water bath and the solid collected by filtration, washing with ice-cold cyclohexane. The residue was dried in vacuo at 50° C. to give the title compound (water retained, 11.1 g). 1H NMR (300 MHz, d4-MeOD): 2.12 (3H, s), 6.38 (1H, dd, J=2.3, 8.0 Hz), 6.44 (1H, d, J=2.3 Hz), 7.02 (1H, d, J=8.1 Hz).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09440974B2uspto-grants-2016_09