Reacción #84802

Ecuación de reacción

methyl 2-(4-aminophenyl)-2-methoxyacetate

3-chloropropane-1-sulfonyl chloride

→

methyl 2-(4-(3-chloropropylsulfonamido)phenyl)-2-methoxyacetate

Rendimiento 99.9%

Disolventes

pyridine

H2O

HCl

brine

Condiciones de reacción

Tratamiento posterior

1. 1
   OtroThe exothermic reaction
2. 2
   Temperaturawas cooled briefly over a cold H2O bath
3. 3
   Extracciónextracted with EtOAc
4. 4
   LavadoThe combined organics were washed with 1 M HCl, H2O and brine
5. 5
   Secadothen dried over Na2SO4
6. 6
   Concentraciónconcentrated in vacuo

Procedimiento

To a solution of methyl 2-(4-aminophenyl)-2-methoxyacetate (0.6 g, 3.07 mmol) in anhydrous pyridine (6 mL) under argon was added 3-chloropropane-1-sulfonyl chloride (0.5 mL, 4.11 mmol) dropwise. The exothermic reaction was cooled briefly over a cold H2O bath. After stirring for 1 hr, the reaction was diluted with H2O, 1 M HCl and brine and extracted with EtOAc. The combined organics were washed with 1 M HCl, H2O and brine then dried over Na2SO4 and concentrated in vacuo to give methyl 2-(4-(3-chloropropylsulfonamido)phenyl)-2-methoxyacetate as an orange oil (1.03 g, quant. yield). The product was used without further purification.

Fuente