تفاعل #55981

ord-75b59b82f4c14b1198acd65eb41b7dfa

المتفاعلات

الكواشف

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ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    غسيلTo sodium hydride, 0.91 g, (22.3 mmol) (washed with hexane)
  2. 2
    workup.ADDITIONis added, under nitrogen
  3. 3
    درجة الحرارةThe suspension is then cooled in an ice bath
  4. 4
    درجة الحرارةthe solution is refluxed for 3 days
  5. 5
    استخلاصextracted with ether
  6. 6
    غسيلwashed with 5% sodium hydroxide (2×), water (3×) and brine
  7. 7
    تجفيفdried over magnesium sulfate
  8. 8
    تركيزconcentrated
  9. 9
    غسيلThe residue is finally washed with 100 ml cold (ice bath) hexane

الإجراء التجريبي

To sodium hydride, 0.91 g, (22.3 mmol) (washed with hexane) is added, under nitrogen, 8 ml of tetrahydrofuran. The suspension is then cooled in an ice bath. Thiophenol (2.32 g, 21.1 mmol) in 8 ml of tetrahydrofuran is added dropwise over 30 minutes, after which 4 ml of hexamethylphosphorictriamide is added. The solution is added dropwise over 15 hr to 5 g (21.1 mmol) 2,6-dibromopyridine in 8 ml tetrahydrofuran and 2 ml hexamethylphosphorictriamide at 24°. The reaction mixture is stirred overnight under nitrogen. After addition of 2 ml hexamethylphosphorictriamide, the solution is refluxed for 3 days, then diluted with water and extracted with ether, washed with 5% sodium hydroxide (2×), water (3×) and brine, dried over magnesium sulfate and concentrated. The residue is finally washed with 100 ml cold (ice bath) hexane to give 2-bromo-6-phenylthiopyridine, m.p. 47°.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04223033uspto-grants-1980_09