Reacción #51200

ord-ed79363d7c4b4e89bde6a718f51e6b66

Ecuación de reacción

COc1ccc(C=O)cc1
4-Methoxy-benzaldehyde
c1ccncc1
pyridine
O=S(=O)(Cl)Cl
sulfuryl chloride
COc1ccc(CCCN)cc1Cl
title product
Rendimiento 77.0%
COc1ccc(CCCN)cc1Cl
3-(4-Methoxy-3-chlorophenyl)-1-propylamine
Rendimiento 77.0%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturamaintaining
  2. 2
    Otrothe internal temperature of the reaction at between 25 and 30° C
  3. 3
    Temperaturawarmed to 70° C. for 4 h
  4. 4
    OtroExcess reagents were removed by evaporation in vacuo
  5. 5
    workup.ADDITIONpoured onto 500 ml hexane with vigorous stirring, from which the product
  6. 6
    Otroprecipitates
  7. 7
    FiltraciónThe solid was filtered off
  8. 8
    Lavadowashed with hexane
  9. 9
    Otrodried in vacuo

Procedimiento

4-Methoxy-benzaldehyde (Aldrich) (42 g, 0.31 mole) and pyridine (0.6 ml, catalytic) were stirred together under nitrogen and sulfuryl chloride (51 g, 0.37 mole) added over 30 min, maintaining the internal temperature of the reaction at between 25 and 30° C. There was a vigorous evolution of gas. The mixture was stirred at room temperature for a further 30 min, and then warmed to 70° C. for 4 h. Excess reagents were removed by evaporation in vacuo and the residue taken up in 50 ml diisopropyl ether and poured onto 500 ml hexane with vigorous stirring, from which the product precipitates. The solid was filtered off and washed with hexane and then dried in vacuo to give the title product (40.3 g, 77%), m.p. 55-56° C.; 1HNMR (400 MHz, CDCl3) δ: 3.99 (s, 3H), 7.05 (dd, 1H), 7.91 (d, 1H), 9.86 (s, 1H); Anal. Found: C, 56.13; H, 4.14%. C8H7ClO2 requires C, 56.33; H, 4.14%.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06849649B2uspto-grants-2005_02