Reacción #4288

ord-e9ac2303bc5d496eaac98b7e1bc15dcc

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe isopropylamine was removed in a rotary evaporator
  2. 2
    Otrothe residue partitioned between chloroform and 5% sodium hydroxide
  3. 3
    OtroThe chloroform was removed by rotary evaporator
  4. 4
    Otroto give an oil

Procedimiento

A solution of 151.46 g (0.548 mole) of methanesulfonic acid[2-[(3,4-dichlorophenyl)thio]ethyl]ester in 100 ml of isopropylamine was heated overnight in a bomb at 100° C. The isopropylamine was removed in a rotary evaporator and the residue partitioned between chloroform and 5% sodium hydroxide. The chloroform was removed by rotary evaporator to give an oil, the free base of the title compound. The oil was dissolved in methanol and converted to the hydrochloride salt with ethereal hydrogen chloride. Recrystallization of the salt from methanol-diethyl ether gave 101.53 g (61.6%) of white crystalline product, m.p. 132°-133.5° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04724235uspto-grants-1988_02