Реакция #1244243

ord-ec3e90af26954903a140c8a4b7005bb8

Уравнение реакции

OCC[O][Na]
HOCH2CH2ONa
CO
methanol
O=S(=O)(F)CCCl
FSO2CH2CH2Cl
C1CCOC1
THF
O=S(=O)(F)CCOCCO
crude product
O=S(=O)(F)CCOCCO
FSO2CH2CH2OCH2CH2OH

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураunder cooling with ice bath
  2. 2
    Температураwhile maintaining the internal temperature
  3. 3
    Другоеto be at most 10° C
  4. 4
    workup.ADDITIONAfter completion of the dropwise addition, it
  5. 5
    workup.STIRRINGwas stirred at room temperature for 2 hours
  6. 6
    workup.ADDITIONwas added
  7. 7
    ДругоеThe obtained crude liquid
  8. 8
    Другоеwas subjected to liquid separation
  9. 9
    Экстракцияthe obtained aqueous layer was extracted with dichloromethane (124 g)
  10. 10
    ЭкстракцияThe separated aqueous layer was further extracted with dichloromethane (126 g)
  11. 11
    СушкаIt was dried over magnesium sulfate
  12. 12
    Фильтрацияafter filtration
  13. 13
    workup.DISTILLATIONthe solvent was distilled off

Методика

Into a round flask, HO(CH2)2OH (140.9 g) and a methanol solution of sodium methylate (28 wt %, 96.4 g) were charged and stirred, and heated under reduced pressure to distill off methanol thereby to obtain a solution of HOCH2CH2ONa. It was confirmed by GC that no methanol remained in the reaction solution. Into a four necked flask, FSO2CH2CH2Cl (50 g) and THF (100 mL) were charged and stirred under cooling with ice bath, and the previously obtained solution of HOCH2CH2ONa was dropwise added thereto over a period of 2.5 hours, while maintaining the internal temperature to be at most 10° C. After completion of the dropwise addition, it was stirred at room temperature for 2 hours and then added to water (400 mL), and dichloromethane (183 g) was added. The obtained crude liquid was subjected to liquid separation, and the obtained aqueous layer was extracted with dichloromethane (124 g). The separated aqueous layer was further extracted with dichloromethane (126 g), and the organic layers were put together. It was dried over magnesium sulfate, and after filtration, the solvent was distilled off to obtain a crude product (47.1 g). The obtained crude liquid was used for the next step without carrying out purification.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: USRE041806E1uspto-grants-2010_10