Reacción #640537
ord-2e69f8efd29f484b93949c4b6aa97162
Ecuación de reacción
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1Temperaturaheated
- 2TemperaturaThe reaction was cooled
- 3Otrothe organic layer separated
- 4Extracciónextracted with ethyl acetate
- 5Lavadowashed with water, brine
- 6Secadodried over magnesium sulfate
- 7Filtraciónfiltered
- 8Concentraciónconcentrated
- 9Otroto yield 0.5 g of crude material
- 10ConcentraciónThe filtrate was concentrated
- 11Otrorecrystallized fom diethyl ether/hexane
Procedimiento
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).