반응 #96206

ord-985a842879254bc6be6e130eaec6c084

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    여과filtered
  2. 2
    세척The solid residue was washed with anhydrous diethyl ether (2×20 ml)
  3. 3
    건조dried over phosphorus pentoxide at a pressure of 0.01 mg Hg for 48 hours

실험 절차

A stirred solution of 1-(3,5-bistrifluoromethylphenyl)-3-(4-tert-butylpiperidino)prop-1-yne (0.98 g) in anhydrous diethyl ether (50 ml) was treated with a solution of sulphuric acid (e.g. 1.84) in anhydrous diethyl ether (0.25 molar solution; 10 ml). The mixture was allowed to stand for 30 minutes and then filtered. The solid residue was washed with anhydrous diethyl ether (2×20 ml) and dried over phosphorus pentoxide at a pressure of 0.01 mg Hg for 48 hours, to give 1-(3,5-bistrifluoromethylphenyl)-3-(4-tert-butylpiperidino)prop-1-yne hydrogensulphate (1.15 g), m.p. 221°-222° C. in the form of a white powder which had the elementary analysis C: 49.1%; H: 5.02%; N: 2.76% (C20H25F6NO4S requires C: 49.07%; H: 5.15%; N: 2.86%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04347252uspto-grants-1982_08