Reaktion #1244243
ord-ec3e90af26954903a140c8a4b7005bb8
Reaktionsgleichung
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1Temperaturunder cooling with ice bath
- 2Temperaturwhile maintaining the internal temperature
- 3Sonstigeto be at most 10° C
- 4workup.ADDITIONAfter completion of the dropwise addition, it
- 5workup.STIRRINGwas stirred at room temperature for 2 hours
- 6workup.ADDITIONwas added
- 7SonstigeThe obtained crude liquid
- 8Sonstigewas subjected to liquid separation
- 9Extraktionthe obtained aqueous layer was extracted with dichloromethane (124 g)
- 10ExtraktionThe separated aqueous layer was further extracted with dichloromethane (126 g)
- 11TrocknenIt was dried over magnesium sulfate
- 12Filtrationafter filtration
- 13workup.DISTILLATIONthe solvent was distilled off
Vorschrift
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.