Reacción #1762427
ord-542c6c5c9e7d4e0ba9e6d18b5578b169
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1workup.ADDITIONAfter addition
- 2Otrothe ice bath was removed
- 3TemperaturaThe mixture was cooled in an ice bath
- 4Otroquenched
- 5workup.ADDITIONby adding saturated sodium bicarbonate until the mixture
- 6workup.ADDITIONMore DCM (400 mL) was added
- 7Otrothe organic layer was separated
- 8Lavadowashed with brine
- 9Otrodried
- 10Concentraciónconcentrated under vacuum
- 11workup.DISSOLUTIONThe crude product (6.5 g) was dissolved in 50 mL of hot MeOH
- 12TemperaturaAfter cooling
- 13Filtraciónthe crystallized product was collected by filtration
- 14Lavadowashed once with MeOH
Procedimiento
Boron trichloride methyl sulfide complex (51 mL, 2.0 M solution in DCM) was added to 7.4 (8.2 g, 17 mmol) in DCM (100 mL) at 0° C. After addition, the ice bath was removed, and the mixture was stirred at room temperature for 7 hours. The mixture was cooled in an ice bath and quenched by adding saturated sodium bicarbonate until the mixture was neutralized. More DCM (400 mL) was added, and the organic layer was separated, washed with brine, dried, and concentrated under vacuum. The crude product (6.5 g) was dissolved in 50 mL of hot MeOH. After cooling, the crystallized product was collected by filtration and washed once with MeOH to give 7.5 (4.2 g). The filtrate was concentrated, and the solid that formed was collected and washed to give an additional 1.2 g of compound 7.5. MS ESI (pos.) m/e: 393 (M+H). 1H NMR (CDCl3) δ 8.29 (d, 1H), 7.30 (m, 3H), 7.20 (d, 2H), 7.15 (d, 2H), 6.95 (d, 2H), 6.14 (d, 1H), 4.71 (dd, 1H), 4.63 (m, 1H), 4.16 (d, 2H), 4.00 (dd, 1H), 3.54 (dd, 1H), 3.21 (dd, 1H), 2.76 (dd, 1H).