تفاعل #80652

ord-8fdd181152aa46cabb863b3fa755a65e

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةwas heated
  2. 2
    درجة الحرارةat reflux for 24 h
  3. 3
    استخلاصThe mixture was extracted with hexanes
  4. 4
    غسيلwashed successively with water, saturated NaHCO3, water again
  5. 5
    تجفيفsaturated NaCl and then dried (MgSO4)
  6. 6
    أخرىThe solvent was removed in vacuo
  7. 7
    أخرىthe residue purified by flash chromatography (silica; hexanes)

الإجراء التجريبي

A mixture of 500 mg (1.49 mmol) of 4-bromo-2-(1,1,3-trimethyl-3-hydroxybutyl) thiophenol (Compound 32) and 8 ml of 20 percent aqueous H2SO4 was heated at reflux for 24 h. The mixture was extracted with hexanes, the organic extracts were combined and washed successively with water, saturated NaHCO3, water again, saturated NaCl and then dried (MgSO4). The solvent was removed in vacuo and the residue purified by flash chromatography (silica; hexanes) to give the title compound as a colorless oil. PMR (CDCl3): & 1.35 (6H, s), 1.40 (6H, s), 1.93 (2H, s), 7.17 (1H, dd, J-8.4 Hz, 2.1 Hz), 7.23 (1H, d, J-8.4 Hz), 7.26 (1H, d, J-2.1 Hz). MS exact mass, m/e 16 284.0221 (calcd. for C13H17S Br, 284.0234).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05616597uspto-grants-1997_04