Reacción #164124

Ecuación de reacción

ether

4-bromoanisole

ether

ether

8-dimethylamino-1,4-dioxa-spiro[4.5]decane-8-carbonitrile

→

desired product

[8-(4-methoxy-phenyl)-1,4-dioxa-spiro[4.5]dec-8-yl]-dimethylamine

Disolventes

THF

Condiciones de reacción

Tratamiento posterior

1. 1
   Temperaturaheated
2. 2
   OtroThe solution formed
3. 3
   workup.ADDITIONuntil boiling during the addition
4. 4
   OtroA precipitate separated out
5. 5
   workup.STIRRINGthe batch was stirred overnight at RT
6. 6
   workup.ADDITIONThe solution was mixed with NH4Cl solution with ice cooling
7. 7
   Otrothe phases were separated
8. 8
   Extracciónthe aqueous phase extracted three times with ether
9. 9
   Lavadothe combined organic phases washed with saturated NaCl solution and water
10. 10
    Secadodried over Na2SO4
11. 11
    Concentraciónconcentrated to low volume in a vacuum

Procedimiento

Magnesium (3.65 g, 150 mmol) and an iodine crystal were provided in a nitrogen atmosphere and heated. Abs. ether (10 mL) was then added and a solution of 4-bromoanisole (18.8 mL, 150 mmol) in abs. ether (150 mL) was added in drops so that the ether lightly boiled. The solution formed was subsequently stirred for 1 h at RT and then mixed in drops with a solution of 8-dimethylamino-1,4-dioxa-spiro[4.5]decane-8-carbonitrile (10.5 g, 50.0 mmol) in abs. THF (100 mL), and the solution heated to 37-40° C. until boiling during the addition. A precipitate separated out and the batch was stirred overnight at RT. The solution was mixed with NH4Cl solution with ice cooling, the phases were separated, the aqueous phase extracted three times with ether, the combined organic phases washed with saturated NaCl solution and water, dried over Na2SO4 and concentrated to low volume in a vacuum. Flash chromatography of the residue with ethyl acetate/methanol (20:1→9:1→4:1→1:4→MeOH) gave the desired product.

Fuente