تفاعل #65588

ord-c7bedd84b32442cfa1e54c07cd4c8dd1

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe reaction mixture was quenched with 1N HCl
  2. 2
    أخرىthe layers separated
  3. 3
    تجفيفthe organic fraction dried over MgSO4
  4. 4
    ترشيحfiltered
  5. 5
    أخرىchromatographed
  6. 6
    أخرىto give a yellow solid

الإجراء التجريبي

To a dry flask containing 40 mL of chloroform was added 1.87 g (18.7 mmol) of tetronic acid, 2.29 g (18.7 mmol) of 4-N,N-dimethylaminopyridine, 2.6 mL (18.7 mmol) of triethylamine followed by 4.4 g (18.7 mmol) of 2-cyclododecylethyl isocyanate. The reaction mixture was allowed to stir overnight at room temperature, after which time a small amount of starting materials was still evident by TLC. The reaction mixture was quenched with 1N HCl, the layers separated, the organic fraction dried over MgSO4, filtered, and stripped of solvent. The residue was flash chromatographed using acidic silica gel eluting with 25% EtOAc/hexane to give a yellow solid. M.P. 135°-137° C. Spectral data follow: 1H NMR (DMSO-d6) δ 8.05 (bs, 1H), 4.6 (s, 2H), 4.2 (bs, 10H), 3.25 (t, 2H), 2.5 (s, 3H), 1.2-1.4 (bm, >20H); IR (KBr) 3340, 2920, 2850 (C--H), 1750, 1650 cm-1 (C=0);

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05420153uspto-grants-1995_05