Reacción #55511

ord-db111377924643b9a7c91b19da1e9bd3

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.WAIT, then at 25° for 15 hr
  2. 2
    Filtraciónfiltered
  3. 3
    workup.DISSOLUTIONThe resulting solid was dissolved in methylene chloride
  4. 4
    Secadodried with magnesium sulfate
  5. 5
    Otroevaporated

Procedimiento

12 Grams (0.16 mole) of chloroacetonitrile was added to a stirred suspension of 6.2 g (0.04 mole) of 2-mercaptonicotinic acid, 8.0 g (0.08 mole) of potassium bicarbonate, and 20 g (0.12 mole) of potassium iodide in 100 ml of dimethylformamide at 10° under nitrogen. The reaction was stirred at 10° for 7 hr., then at 25° for 15 hr. The reaction mixture was then poured into water, saturated with sodium chloride and filtered. The resulting solid was dissolved in methylene chloride, dried with magnesium sulfate and evaporated to give 7.5 g of cyanomethyl 2-(cyanomethylthio)nicotinate. m.p. 140°-143° C. NMR (DMSO) δ3.3(s,2); 4.3(s,2); 6.4(dd,1); 7.4(dd,1); 7.8(dd,1).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04220776uspto-grants-1980_09