Réaction #640537
ord-2e69f8efd29f484b93949c4b6aa97162
Équation de réaction
Conditions de réaction
Traitement
- 1Températureheated
- 2TempératureThe reaction was cooled
- 3Autrethe organic layer separated
- 4Extractionextracted with ethyl acetate
- 5Lavagewashed with water, brine
- 6Séchagedried over magnesium sulfate
- 7Filtrationfiltered
- 8Concentrationconcentrated
- 9Autreto yield 0.5 g of crude material
- 10ConcentrationThe filtrate was concentrated
- 11Autrerecrystallized fom diethyl ether/hexane
Mode opératoire
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).