Reaktion #492854

ord-0ae4d1ffe7d646adb62d32b1a55ac5e5

Reaktionsgleichung

O
Water
[BH4-].[Na+]
sodium borohydride
CC(C)Oc1ccc(S(N)(=O)=O)cc1[N+](=O)[O-]
4-isopropoxy-3-nitro-benzenesulfonamide
CC(C)Oc1ccc(S(N)(=O)=O)cc1[N+](=O)[O-]
4-Isopropoxy-3-nitro-benzenesulfonamide
[BH4-].[Na+]
Sodium borohydride
CC(C)Oc1ccc(S(N)(=O)=O)cc1N
title compound
CC(C)Oc1ccc(S(N)(=O)=O)cc1N
3-Amino-4-isopropoxy-benzenesulfonamide

Lösungsmittel

Reaktionsbedingungen

Temperatur
23°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe mixture was cooled to 0° C.
  2. 2
    workup.STIRRINGThe resulting black suspension was stirred for 30 min at 23° C
  3. 3
    Sonstigeto quench excess NaBH4
  4. 4
    workup.ADDITIONfollowed by addition of saturated aqueous NaHCO3
  5. 5
    ExtraktionThe product was extracted with dichloromethane
  6. 6
    Waschenthe organic phase was washed with brine
  7. 7
    Trocknendried with Na2SO4
  8. 8
    Sonstigeevaporated

Vorschrift

Sodium borohydride (1.88 g, 49.6 mmol) was added slowly to a solution of nickel (II) chloride hexahydrate (3.93 g, 16.5 mmol) in methanol (60 mL) at 0° C. and the resulting black suspension was stirred for 30 min at 23° C. The mixture was cooled to 0° C. and 4-isopropoxy-3-nitro-benzenesulfonamide (8.6 g, 33.0 mmol, example 2, step c) was added followed by sodium borohydride (4.38 g, 115.6 mmol). The resulting black suspension was stirred for 30 min at 23° C. Water was added to the reaction mixture to quench excess NaBH4, followed by addition of saturated aqueous NaHCO3. The product was extracted with dichloromethane and the organic phase was washed with brine, dried with Na2SO4 and evaporated to give the title compound.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08753857B2uspto-grants-2014_06