Реакция #51862

ord-7caf2594e6bf4d3d8d2fcf66f8ea9bb5

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.DISSOLUTIONThe mixture completely dissolved
  2. 2
    ДругоеThe volatile fractions were removed in vacuo and water (30 cm3)
  3. 3
    workup.ADDITIONwas added to the mixture
  4. 4
    Экстракцияwas extracted with dichloromethane (3×30 cm3)
  5. 5
    ПромывкаThe combined extracts were washed with brine (30 cm3)
  6. 6
    Сушкаdried over sodium sulfate, vacuum
  7. 7
    Фильтрацияfiltered
  8. 8
    Другоеthe filtrate volatile fractions removed in vacuo to a crude golden oil
  9. 9
    ДругоеThe oil was triturated in Et2O (30 cm3)
  10. 10
    Фильтрацияvacuum filtered
  11. 11
    Промывкаwashed with Et2O (2×10 cm3) and vacuum
  12. 12
    Другоеdried to constant weight

Методика

To a stirred mixture 2-[4,5-dimethoxy-2-(morpholine-4-sulfonyl)-phenyl]-pent-4-enoic acid benzyl ester (3.25 g, 6.83 mmol) in methanol (28 cm3) under an atmosphere of dry nitrogen was added sodium hydroxide (820 mg, 20.5 mmol) dissolved in water (7 cm3). The mixture completely dissolved while stirring at ambient temperature for 20 hours. The volatile fractions were removed in vacuo and water (30 cm3) was added to the mixture. The aqueous mixture acidified with 6N HCl to pH 1.0 and was extracted with dichloromethane (3×30 cm3). The combined extracts were washed with brine (30 cm3), dried over sodium sulfate, vacuum filtered and the filtrate volatile fractions removed in vacuo to a crude golden oil. The oil was triturated in Et2O (30 cm3), vacuum filtered, washed with Et2O (2×10 cm3) and vacuum dried to constant weight to afford the title compound as (2.30 g, 87.54%) with a positive ion ESI (M+H)+386.2.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06852713B2uspto-grants-2005_02