تفاعل #69509

ord-872bb89e4f994941b3711d549ccabc83

الكواشف

لا شيء

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGthe resulting mixture was stirred for 8.5 hours
  2. 2
    workup.STIRRINGAfter thoroughly shaking the mixture
  3. 3
    أخرىthe organic layer was separated
  4. 4
    غسيلthe organic layer was washed with brine
  5. 5
    تجفيفdried over anhydrous magnesium sulfate
  6. 6
    ترشيحThe mixture was filtered
  7. 7
    workup.DISTILLATIONthe solvent in the filtrate was distilled off under reduced pressure
  8. 8
    أخرىThe residue was purified by silica gel column chromatography (a mixed solvent of n-heptane and ethyl acetate

الإجراء التجريبي

To a mixture of 3-hydroxytetrahydrofuran (7.00 g, 79.5 mmol) and pyridine (100 mL), was added p-toluenesulfonyl chloride (18.2 g, 95.4 mmol) while stirring at room temperature, and the resulting mixture was stirred for 8.5 hours. To the mixture, were added water and ethyl acetate. After thoroughly shaking the mixture, the organic layer was separated, and the organic layer was washed with brine and dried over anhydrous magnesium sulfate. The mixture was filtered, and then the solvent in the filtrate was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (a mixed solvent of n-heptane and ethyl acetate: n-heptane/ethyl acetate=4/1) to obtain the title compound (13.0 g, 53.7 mmol).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08530504B2uspto-grants-2013_09