Methanol → Ethanesulfonyl fluoride, 2-(2-hydroxyethoxy)-

HRID 1157061Notes

Reaction equation

HRID 1157061 reaction equation
CO.[F:3][S:4]([CH2:7][CH2:8]Cl)(=[O:6])=[O:5].C1COCC1.[OH:15][CH2:16][CH2:17][O:18][Na]>ClCCl.O>[F:3][S:4]([CH2:7][CH2:8][O:15][CH2:16][CH2:17][OH:18])(=[O:6])=[O:5]

Participants

7

Procedure

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.

Workup

  1. temperatureunder cooling with ice bath
  2. temperaturewhile maintaining the internal temperature
  3. customto be at most 10° C
  4. additionAfter completion of the dropwise addition, it
  5. stirringwas stirred at room temperature for 2 hours
  6. additionwas added
  7. customThe obtained crude liquid
  8. customwas subjected to liquid separation
  9. extractionthe obtained aqueous layer was extracted with dichloromethane (124 g)
  10. extractionThe separated aqueous layer was further extracted with dichloromethane (126 g)
  11. dry with materialIt was dried over magnesium sulfate
  12. filtrationafter filtration
  13. distillationthe solvent was distilled off

Sources & evidence

ORD record
ord-ec3e90af26954903a140c8a4b7005bb8
Source dataset
uspto-grants-2010_10
Patent number
USRE041806E1

Reaction notes

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