Reaktion #1479

ord-febdc1c7fac448b78a423b7cf31b3624

Reaktionsgleichung

O=S(=O)(O)O
H2SO4
O=[N+]([O-])O
HNO3
O=S(=O)(O)O
H2SO4
CC1(C)CCC(=O)c2ccccc21
3,4-dihydro-4,4-dimethyl-naphthalen-1(2H)-one
CC1(C)CCC(=O)c2cc([N+](=O)[O-])ccc21
title compound
CC1(C)CCC(=O)c2cc([N+](=O)[O-])ccc21
3,4-dihydro-4,4-dimethyl-7-nitro-naphthalen-1(2H)-one

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeat 5° C.
  2. 2
    workup.ADDITIONice was added
  3. 3
    Extraktionthe resulting mixture was extracted with EtOAc
  4. 4
    EinengenThe combined extracts were concentrated under reduced pressure

Vorschrift

To 1.7 mL (3.0g, 30.6 mmol, 18M) H2SO4 at 5° C. (ice-NaCl bath) was slowly added 783.0 mg (4.49 mmol) of 3,4-dihydro-4,4-dimethyl-naphthalen-1(2H)-one. A solution of HNO3 (426.7 mg 6.88 mmol, 0.43 mL, 16M), and 1.31 g (0.013 mol, 0.74 mL, 18M) Of H2SO4 were slowly added. After 20 min, ice was added and the resulting mixture was extracted with EtOAc. The combined extracts were concentrated under reduced pressure to give a yellow oil from which the title compound, a pale yellow solid, was isolated by column chromatography (10% EtOAC/hexanes).

Quelle

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