Реакция #1869153

ord-082ac3331501484a9c124c4ecaa3c4fc

Уравнение реакции

Cl
HCl
CCCCCCCCCC1(CC(=O)OCC)OCCO1
ethyl 3,3-ethylenedioxydodecanoate
O.[Li][OH]
LiOH.H2O
C1CCOC1
THF
CCCCCCCCCC1(CC(=O)O)OCCO1
3,3-ethylenedioxydodecanoic acid
Выход 81.0%

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Экстракцияextracted with ethyl acetate (3×50 mL)
  2. 2
    Промывкаwashed once with brine
  3. 3
    СушкаThe organic phase was dried (MgSO4)
  4. 4
    Концентрированиеconcentrated

Методика

To a 25 mL flask were added ethyl 3,3-ethylenedioxydodecanoate (1.131 g, 3.95 mmol), LiOH.H2O (840 mg, 20 mmol), THF (5 mL), and water (5 mL). The mixture was stirred at room temperature overnight. The solution was acidified by the addition of 1 M HCl (50 mL), and extracted with ethyl acetate (3×50 mL). The organic layers were combined and washed once with brine. The organic phase was dried (MgSO4) and concentrated to give 3,3-ethylenedioxydodecanoic acid (0.824 g, 3.19 mmol) in 81% yield. 1H NMR (500 MHz, CDCl3) δ 0.88 (t, J=7 Hz, 3H), 1.20-1.44 (m, 14H), 1.72-1.80 (m, 2H), 2.72 (s, 2H), 3.98-4.10 (m, 4H); 13C NMR (125 MHz, CDCl3) δ 13.9, 22.5, 23.3, 29.13, 29.35, 29.39, 29.50, 31.7, 37.5, 42.2, 64.9 (2 C), 109.2, 174.8.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07498292B2uspto-grants-2009_03