تفاعل #216826

ord-b2d7135e89b9457fbf63c1297f0d6f66

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe organic phase is separated
  2. 2
    تجفيفdried over anhydrous magnesium sulfate
  3. 3
    تركيزconcentrated in vacuo
  4. 4
    أخرىto obtain a residue

الإجراء التجريبي

A solution of 3-bromo-5-(p-chlorophenyl)-2-(trifluoromethyl)-4-[(trifluoromethyl)thio]pyrrole (0.6 g, 1.4 mmol) and potassium tert-butoxide (0.19 g, 1.7 mmol) in tetrahydrofuran is stirred for 15 minutes, treated with chloromethyl ethyl ether (0.16 g, 1.7 mmol), stirred for 30 minutes and diluted with an ether/water mixture. The organic phase is separated, dried over anhydrous magnesium sulfate and concentrated in vacuo to obtain a residue. Chromatography of the residue using silica gel and a 1:9 ethyl acetate/hexanes solution gives the title product as an amber oil which is identified by 1HNMR and 13CNMR spectral analyses.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05468877uspto-grants-1995_11