Реакция #2146707

ord-c4118500adee4f2098228f0201e4ab83

Уравнение реакции

[I-].[K+]
potassium iodide
Cc1ccc(S(=O)(=O)Cl)cc1
p-toluenesulfonyl chloride
OCCCO
1,3-propanediol
Cc1ccc(S(=O)(=O)OCCCO)cc1
1,3-propanediol mono-p-toluenesulfonate
Выход 53.5%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ФильтрацияInsoluble matters were filtered out of the reaction mixture
  2. 2
    Промывкаwere washed with ethyl acetate
  3. 3
    Концентрированиеthe mixture was concentrated
  4. 4
    ДругоеThe resulting crude product was purified with flash silica gel column chromatography (elution solvent: hexane/ethyl acetate=3/2 to 1/1)

Методика

1.45 mL (corresponding to 20.0 mmol) of 1,3-propanediol was dissolved in 200 mL of methylene chloride. To this solution under an ice bath, 6.96 g (corresponding to 30.0 mmol) of silver oxide, 666 mg (corresponding to 4.0 mmol) of potassium iodide and 4.21 g (corresponding to 22.0 mmol) of p-toluenesulfonyl chloride were added. The resulting mixture was stirred at room temperature for 3 hours. Insoluble matters were filtered out of the reaction mixture, and were washed with ethyl acetate. The washings were combined with the filtrate, and the mixture was concentrated. The resulting crude product was purified with flash silica gel column chromatography (elution solvent: hexane/ethyl acetate=3/2 to 1/1) to obtain 2.47 g (corresponding to 10.7 mmol) of 1,3-propanediol mono-p-toluenesulfonate (FIG. 1, Step 6).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08277777B2uspto-grants-2012_10