Reacción #43123

ord-f642b3d2bd1945ed90836493516f8c34

Ecuación de reacción

COc1ccc(CCN)cc1
2-(4-Methoxy-phenyl)-ethylamine
O=S(=O)(Cl)Cl
sulfuryl chloride
CCOCC
ether
NCCc1ccc(O)c(Cl)c1
4-(2-Amino-ethyl)-2-chloro-phenol

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Filtraciónthe resulted solid was collected by filtration
  2. 2
    TemperaturaThe solid was heated in 48% aqueous HBr at 135° C. for 4 hours
  3. 3
    Temperaturacooled to 0° C.
  4. 4
    Filtraciónthe crystal was collected by filtration
  5. 5
    Lavadowashed with small amount of methanol

Procedimiento

0.1 mol of 2-(4-Methoxy-phenyl)-ethylamine was dissolved in 200 ml of acetic acid, followed by addition of 1.5 eq. of sulfuryl chloride at 0° to 5° C. The solution was stirred at room temperature for 1 hour. 250 ml of ether was added and the resulted solid was collected by filtration. The solid was heated in 48% aqueous HBr at 135° C. for 4 hours, cooled to 0° C., and the crystal was collected by filtration and washed with small amount of methanol then with ethyl acetate. LC-MS showed the product as HBr salt had the expected M+H+ of 186. 1H NMR (Varian 300 MHz, CD3OD shifts relative to the solvent peak at 3.3 ppm) δ 7.2 (d, 1H) 7.0 (m, 1H) 6.9 (d, 1H) 3.1 (m, 2H) 2.9 (m, 2H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07732444B2uspto-grants-2010_06