Réaction #40294

ord-3ae22f97cb3a4f52b62b49ef8cde42a7

Équation de réaction

Cc1cc(C(C)(C)C)cc(C)c1[N+](=O)[O-]
1-nitro-4-tert-butyl-2,6-dimethylbenzene
Cc1cc(C(C)(C)C)cc(C)c1[N+](=O)[O-]
1-nitro-4-tert-butyl-2,6-dimethylbenzene
[Ca+2].[Cl-].[Cl-]
CaCl2
Cc1cc(C(C)(C)C)cc(C)c1N
brown oil
Rendement 93.2%
Cc1cc(C(C)(C)C)cc(C)c1N
2,6-dimethyl-4-tert-butylaniline
Rendement 93.2%

Conditions de réaction

Température
65°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurecooled to ambient temperature
  2. 2
    Filtrationfiltered
  3. 3
    ExtractionThe filtrate was extracted three times with ether
  4. 4
    Séchagethe organic layer was dried over MgSO4
  5. 5
    AutreRemoval of the solvent

Mode opératoire

Water, 20 mL, was added to a mixture of 12.0 g (58.0 mmol) of 1-nitro-4-tert-butyl-2,6-dimethylbenzene dissolved in 160 mL of ethanol. To the stirring solution of 1-nitro-4-tert-butyl-2,6-dimethylbenzene was added CaCl2, 4.8 g (43.2 mmol), dissolved in 20 mL of water, followed by the addition of zinc powder, 50.0 g (76.5 mmol). The reaction was stirred overnight at 65° C., then cooled to ambient temperature and filtered. The filtrate was extracted three times with ether, and the organic layer was dried over MgSO4. Removal of the solvent gave 9.58 g (93%) of a brown oil. 1H NMR (300 MHz, CDCl3): δ=6.90, s, 2H; 3.40, broad singlet, 2H; 2.11, s, 6H, 1.21, s, 9H.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07727926B2uspto-grants-2010_06