Réaction #1479

ord-febdc1c7fac448b78a423b7cf31b3624

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

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

Mode opératoire

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).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05723666uspto-grants-1998_03