Реакция #1052424

ord-e82fe50325f74afe8e09e121d8c1a2b8

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe crude product was purified by chromatography on silica eluting with 0-4% ethanol in diethyl ether
  2. 2
    ЭкстракцияThe resulting light brown oil (3.89 g) was extracted into a mixture of hexane and diethyl ether
  3. 3
    workup.ADDITIONtreated with ethereal HCl

Методика

The title compound was prepared in a similar manner to Example 26 from (±) cis 2-amino-1-indanol (2.24 g, 15.0 mmol), sodium hydride (0.54 g of an 80% dispersion in oil; 18.0 mmol) and 1,2-dichloro-4-fluorobenzene (2.97 g, 18.0 mmol). The crude product was purified by chromatography on silica eluting with 0-4% ethanol in diethyl ether. The resulting light brown oil (3.89 g) was extracted into a mixture of hexane and diethyl ether and treated with ethereal HCl to give the hydrochloride salt. Recrystallisation afforded the title compound as a colourless solid, m.p. 214°-215° C. (dec) (from methanol/ethyl acetate/diethyl ether).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05773463uspto-grants-1998_06