Reacción #47218
ord-badb8b1ae3714445bff68784f825db23
Ecuación de reacción
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1Temperaturathe mixture was heated to 120° C. for 4 h
- 2TemperaturaThe mixture was cooled down to room temperature
- 3Extracciónextracted with ethyl ether
- 4LavadoThe combined ether layers were washed with 1M NaOH, water, brine
- 5Secadodried over anhydrous Na2SO4
- 6Filtraciónfiltered
- 7Otrosolvent removed under vacuum
- 8OtroThe crude product was absorbed onto silica
- 9Otropurified by flash column (silicagel, hexane
Procedimiento
To a heavy walled vial containing methyl 2-chloro-3,4-dihydroxybenzoate (899.8 mg, 4.4 mmol, 1 equiv.) in 13 mL DMF was added KF (1.29 g, 22.2 mmol, 5 equiv.) and the mixture was stirred at room temperature for 30 min. Dibromomethane (0.375 mL, 5.3 mmol, 1.2 equiv.) was added and the mixture was heated to 120° C. for 4 h. The mixture was cooled down to room temperature, diluted with water, and extracted with ethyl ether. The combined ether layers were washed with 1M NaOH, water, brine, dried over anhydrous Na2SO4, filtered and solvent removed under vacuum. The crude product was absorbed onto silica and purified by flash column (silicagel, hexane:ethyl acetate 8 Å to give 395.8 mg (42%) of methyl 4-chlorobenzo[d][1,3]dioxole-5-carboxylate as a colorless crystalline solid. See Tetrahedron Lett. 38: 3361-3364 (1978); U.S. Patent Appl. Publication No. 20050009867.