تفاعل #463201

ord-febc5d645da04ac8b53a1c2e92ce0655

معادلة التفاعل

CN[C@@H](C)[C@@H](O)c1ccccc1
(+)-pseudoephedrine
CCN(CC)CC
triethylamine
O=C(Cl)Cc1ccccc1
phenylacetyl chloride
CC(C(O)c1ccccc1)N(C)C(=O)Cc1ccccc1
phenylacetamide
المردود 75.0%
CC(C(O)c1ccccc1)N(C)C(=O)Cc1ccccc1
N-(2-hydroxy-1-methyl-2-phenylethyl)-N-methyl benzeneacetamide
المردود 75.0%

الكواشف

لا شيء

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىA dry 1 L round-bottomed flask equipped with a magnetic stirrer
  2. 2
    أخرىthe reaction was quenched with saturated sodium bicarbonate
  3. 3
    استخلاصThe amide was extracted from brine (1 L) with ethyl acetate (400 mL, 130 mL, 130 mL)
  4. 4
    تجفيفthe organic extracts were dried over sodium sulfate
  5. 5
    أخرىAfter removal of the solvent under reduced pressure
  6. 6
    أخرىa solid was obtained
  7. 7
    أخرىThe solid was recrystallized from 2:1:1 ether/dichloromethane/hexanes (500 mL)

الإجراء التجريبي

A dry 1 L round-bottomed flask equipped with a magnetic stirrer was charged (+)-pseudoephedrine (13.92 g, 84.26 mmol, 1.0 equiv), triethylamine (13.39 mL, 96.06 mmol, 1.14 mmol), and tetrahydrofuran (340 mL). The solution was cooled to 0° C. and phenylacetyl chloride (14.33 g, 92.69 mmol, 1.1 equiv) was added via cannula over a 20 minute interval as a solution in tetrahydrofuran (90 mL). After 30 minutes, the reaction was quenched with saturated sodium bicarbonate. The amide was extracted from brine (1 L) with ethyl acetate (400 mL, 130 mL, 130 mL), and the organic extracts were dried over sodium sulfate. After removal of the solvent under reduced pressure, a solid was obtained. The solid was recrystallized from 2:1:1 ether/dichloromethane/hexanes (500 mL), affording the phenylacetamide (17.90 g, 75% yield) as a white powder: mp 145°-146° C.; 1H NMR (300 MHz, C6D6) δ6.9-7.5 (m, 10H), 4.55 (br, 1H), 4.48 (t, 1H, J=7.1 Hz), 4.11 (m, 1H), 3.95 (m, 1H), 3.83 (m, 1H), 3.78 (s, 2H), 3.31 (d, 2H, J=1.3 Hz), 2.76 (s, 3H), 2.12 (s, 3H), 0.95 (d, 3H, J=7.0 Hz), 0.42 (d, 3H, J=6.7 Hz); 13C NMR (75.5 MHz, CDCl3) δ173.1, 172.2, 142.2, 141.4, 135.5, 134.5, 128.7, 128.64, 128.58, 128.3, 128.1, 127.5, 126.73, 126.68, 126.6, 126.3, 76.2, 75.3, 58.6, 41.8, 41.4, 33.3, 27.0, 15.0, 14.3; FTIR (neat film) cm-1 3393 (br, m), 1618 (s), 1494 (m), 1453 (m), 1402 (m); HRMS (FAB) Calcd for C18H22NO2 (MH+): 284. 1652. Found: 284.1646.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05488131uspto-grants-1996_01