反応 #583128

ord-eeae68cc47684094a6bafc9410ab3241

反応方程式

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-1(2H)-naphthalenone
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-1(2H)-naphthalenone

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他at −5° C.
  2. 2
    workup.ADDITIONice was added
  3. 3
    抽出the resulting mixture extracted with EtOAc
  4. 4
    濃縮The combined extracts were concentrated under reduced pressure

実験手順

To 1.7 ml (3.0 g, 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-1(2H)-naphthalenone. A solution of 426.7 mg (6.88 mmol, 0.43 ml, 16M) HNO3, and 1.31 g (0.013 mol, 0.74 ml, 18 M) H2SO4 was slowly added. After 20 minutes, ice was added and the resulting mixture extracted with EtOAc. The combined extracts were concentrated under reduced pressure to give a residue from which the title compound, a pale yellow solid, was isolated by column chromatography (10% EtOAC/hexanes). 1H NMR (CDCl3): δ 8.83 (1H, d, J=2.6 Hz), 8.31 (1H, dd, J=2.8, 8.9 Hz), 7.62 (1H, d, J=8.7 Hz), 2.81 (2H, t, J=6.5 Hz), 2.08 (2H, t, J=6.5 Hz), 1.45 (6H, s).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06942980B1uspto-grants-2005_09