反応 #698216

ord-b718762ba7754ee4b52625276fc762b6

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-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

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.ADDITIONice was added
  2. 2
    抽出the resulting mixture was extracted with EtOAc
  3. 3
    濃縮The combined extracts were concentrated under reduced pressure

実験手順

To 1.7 mL (3.0g, 30.6 mmol, 18M) H2SO4 at -5C. (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, 18 M) 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).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05998655uspto-grants-1999_12