Реакция #5345

ord-86ae5c67c1df403db2f7cf7d7103c33f

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Экстракцияextracted with two 100 mL portions of methylene chloride
  2. 2
    СушкаThe combined organic layers are dried over MgSO4
  3. 3
    Концентрированиеconcentrated in vacuo
  4. 4
    Другоеaffording crude compound

Методика

To a stirring solution of 1.6 g (16 mmol) of tetronic acid in 75 mL of methylene chloride is added 2.5 mL (17.86 mmol) of triethylamine and 640 mg of 4-dimethylaminopyridine at 0° C. Next, 5.0 g (17.6 mmol) of stearoyl chloride is added and the reaction is stirred overnight at room temperature. The reaction is acidified with 1.0N HCl and extracted with two 100 mL portions of methylene chloride. The combined organic layers are dried over MgSO4 and concentrated in vacuo affording crude compound. Pure material was obtained by trituration with ethyl acetate as affording 3.3 g (58%) of 4-hydroxy-3-(1-oxooctadecyl)-2(5H)-furanone.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05242945uspto-grants-1993_09