Reacción #1833236

Ecuación de reacción

sodium iodide

2,2-Difluoro-6-methoxybenzo[d][1,3]dioxol-5-amine

HCl

NaHSO3

sodium nitrite

→

title compound

Rendimiento 83.1%

2,2-Difluoro-5-iodo-6-methoxybenzo[d][1,3]dioxole

Rendimiento 83.1%

Disolventes

water

dichloromethane

dichloromethane

water

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.ADDITIONadded in portions
2. 2
   Otroto form a loose white slurry
3. 3
   workup.WAITAfter 45 min
4. 4
   ExtracciónThe separated aqueous phase was extracted with dichloromethane (30 mL)
5. 5
   Lavadothe combined extracts were washed with saturated NaCl (15 mL)
6. 6
   Secadodried (Na2SO4)
7. 7
   Otroevaporated
8. 8
   OtroThe material was purified by chromatography on silica with a 0-15% ethyl acetate-hexane gradient

Procedimiento

2,2-Difluoro-6-methoxybenzo[d][1,3]dioxol-5-amine (1.4 g, 6.9 mmol) was dissolved in dichloromethane (5 mL) and added in portions to rapidly stirred concentrated HCl (75 mL) to form a loose white slurry. The mixture was cooled to 0-5° C. and treated in portions with sodium nitrite (710 mg, 10 mmol) in water (10 mL). After 40 min, this mixture was poured as a thin stream into a solution of sodium iodide (3.1 g, 21 mmol) in water (75 mL) rapidly stirred with dichloromethane (50 mL). After 45 min, the mixture was stirred with 15% NaHSO3 solution (20 mL) for 10 min. The separated aqueous phase was extracted with dichloromethane (30 mL), and the combined extracts were washed with saturated NaCl (15 mL), dried (Na2SO4) and evaporated. The material was purified by chromatography on silica with a 0-15% ethyl acetate-hexane gradient to afford the title compound as a white solid (1.8 g, 83%): mp 50-51° C.; 1H NMR (400 MHz, CDCl3) δ 7.45 (s, 1H), 6.69 (s, 1H), 3.86 (s, 3H); 19F NMR (376 MHz, CDCl3) δ −49.81 (s); EIMS m/z 314.

Fuente