Reaktion #1480

ord-c7356141cfe445de9c86a692d1573d44

Reaktionsgleichung

CC1(C)CCC(=O)c2cc([N+](=O)[O-])ccc21
3,4-dihydro-4,4-dimethyl-7-nitro-naphthalen-1(2H)-one
CC1(C)CCC(=O)c2cc([N+](=O)[O-])ccc21
Compound D8
CC1(C)CCC(=O)c2cc([N+](=O)[O-])ccc21
3,4-dihydro-4,4-dimethyl-7-nitro-naphthalen-1(2H)-one
CC1(C)CCC(=O)c2cc(N)ccc21
title compound
CC1(C)CCC(=O)c2cc(N)ccc21
3,4-dihydro-4,4-dimethyl-7-amino-naphthalen-1(2H)-one

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe catalyst was removed by filtration through a pad of Celite
  2. 2
    Einengenthe filtrate concentrated under reduced pressure

Vorschrift

A solution of 230.0 mg (1.05 mmol) 3,4-dihydro-4,4-dimethyl-7-nitro-naphthalen-1(2H)-one (Compound D8) in 5.0 mL of EtOAc was stirred at room temperature with a catalytic amount of 10% Pd-C under 1 atm of H2 for 24 h. The catalyst was removed by filtration through a pad of Celite, and the filtrate concentrated under reduced pressure to give the title compound as a dark green oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05723666uspto-grants-1998_03