Réaction #1244243

ord-ec3e90af26954903a140c8a4b7005bb8

Équation de réaction

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

Réactifs

Aucun

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températureunder cooling with ice bath
  2. 2
    Températurewhile maintaining the internal temperature
  3. 3
    Autreto 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
    AutreThe obtained crude liquid
  8. 8
    Autrewas subjected to liquid separation
  9. 9
    Extractionthe obtained aqueous layer was extracted with dichloromethane (124 g)
  10. 10
    ExtractionThe separated aqueous layer was further extracted with dichloromethane (126 g)
  11. 11
    SéchageIt was dried over magnesium sulfate
  12. 12
    Filtrationafter filtration
  13. 13
    workup.DISTILLATIONthe solvent was distilled off

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: USRE041806E1uspto-grants-2010_10