Reacción #41299

Ecuación de reacción

isopropylmagnesium chloride

HCl

(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)magnesium bromide

(S)-tert-butyl 1-(methoxy(methyl)amino)-1-oxopropan-2-ylcarbamate

→

(S)-tert-butyl 1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-1-oxopropan-2-ylcarbamate

Disolventes

tert-butyl methyl ether

TBME

water

TBME

THF

THF

THF

Condiciones de reacción

Tratamiento posterior

1. 1
   Otrothe temperature below −10° C
2. 2
   workup.DISSOLUTIONto dissolve
3. 3
   Otroto reach 0° C.
4. 4
   Otroto reach r.t.
5. 5
   workup.ADDITIONwas added
6. 6
   Otrothe mixture was transferred to a separation funnel
7. 7
   LavadoThe ether phases were washed with water, brine
8. 8
   Secadodried (Na2SO4)

Procedimiento

A suspension of (S)-tert-butyl 1-(methoxy(methyl)amino)-1-oxopropan-2-ylcarbamate (3 g, 12.92 mmol) in THF (30 mL) was placed under a protective atmosphere of Argon and cooled down to −15 to −20° C., isopropylmagnesium chloride, 2M in THF (6.5 mL, 13.00 mmol) was added keeping the temperature below −10° C. The slurry started to dissolve, temperature was allowed to reach 0° C., a freshly prepared solution of (2,3-dihydrobenzo[b][1,4]dioxin-6-yl)magnesium bromide, 0.7M in THF (20 mL, 14.00 mmol) was added. The temperature was allowed to reach r.t., the reaction mixture was stirred for 17 h. 1N HCl (300 mL) was cooled on icebath to +10° C., the reaction mixture was poured into the acidic water solution, TBME=tert-butyl methyl ether (300 mL) was added and the mixture was transferred to a separation funnel. The waterphase was backextracted with TBME (200 mL). The ether phases were washed with water, brine and dried (Na2SO4).

Fuente