تفاعل #5386

ord-a06527d7605c46b0b8ec403e13acd486

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe organic layer was isolated
  2. 2
    غسيلwashed with saturated NaHCO3 and 50 mL 1N HCl
  3. 3
    تجفيفdried over MgSO4
  4. 4
    أخرىevaporated
  5. 5
    أخرىto give an oil, which
  6. 6
    أخرىcrystallized rapidly
  7. 7
    workup.ADDITIONafter the addition of 50 mL diethyl ether
  8. 8
    أخرىThe product was isolated by filtration and vacuum
  9. 9
    أخرىdried
  10. 10
    أخرىYield

الإجراء التجريبي

3,4,5-Triacetoxybenzoyl chloride (0.050 mol) was dissolved in 100 mL CH2Cl2 at 0° C. To this was added 2-aminoethyl methacrylate hydrochloride (8.28 g, 0.050 mol), followed by dropwise addition of triethylamine (14.63 mL, 0.105 mol). After 30 min, 100 mL 1N HCl was added with vigorous stirring. The organic layer was isolated, washed with saturated NaHCO3 and 50 mL 1N HCl, dried over MgSO4, and evaporated to give an oil, which crystallized rapidly after the addition of 50 mL diethyl ether. The product was isolated by filtration and vacuum dried. Yield, 17.97 g as a white solid, 88%. 1H NMR (300 MHz, CDCl3), δ1.92 (s, 3H), 2.26 (s, 6H), 2.27 (s, 3H), 3.68 (m, 2H), 4.30 (t, 2H), 5.58 (m, 1H), 6.11 (s, 1H), 6.66 (t, broad, 1H), 7.51 (s, 2H). Anal., calcd for C19H21N1O9C 56.02, H 5.20, N 3.44, found C 55.99, H 5.15, N 3.50.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05244763uspto-grants-1993_09