Реакция #640537

ord-2e69f8efd29f484b93949c4b6aa97162

Уравнение реакции

CCCCCC
hexane
Cc1cccc([N+](=O)[O-])c1I
2-iodo-nitrotoluene
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CCOCC
diethyl ether
Cc1cc([N+](=O)[O-])ccc1C(=O)O
4-nitro-2-methylbenzoic acid
Выход 31.2%

Условия реакции

Температура
70°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураheated
  2. 2
    ТемператураThe reaction was cooled
  3. 3
    Другоеthe organic layer separated
  4. 4
    Экстракцияextracted with ethyl acetate
  5. 5
    Промывкаwashed with water, brine
  6. 6
    Сушкаdried over magnesium sulfate
  7. 7
    Фильтрацияfiltered
  8. 8
    Концентрированиеconcentrated
  9. 9
    Другоеto yield 0.5 g of crude material
  10. 10
    КонцентрированиеThe filtrate was concentrated
  11. 11
    Другоеrecrystallized fom diethyl ether/hexane

Методика

A mixture of 1.0 g (3.8 mmol) of 2-iodo-nitrotoluene, 2.1 g (15.2 mmol) potassium carbonate and 27 mg (0.038 mmol) of palladium(II) dichloride bis(triphenylphosphine) in a mixture of 5 mL of water and 10 mL of N,N-dimethylformamide. This was placed in a Fisher/Porter bottle under 15 psig of carbon monoxideand heated at 70° C. for 16 hours. The solution became homogeneous when heated. The reaction was cooled, diethyl ether and water was added, the organic layer separated and discarded. The aqueous layer was acidified with IN hydrohloric acid, extracted with ethyl acetate, washed with water, brine, dried over magnesium sulfate, filtered and concentrated to yield 0.5 g of crude material. This dissolved in ethyl acetate, hexane added and the resulting brown solid discarded. The filtrate was concentrated, and then recrystallized fom diethyl ether/hexane to afford 215 mg of 4-nitro-2-methylbenzoic acid, m/e=182 (M+H).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: USRE042889E1uspto-grants-2011_11