Water → 2-(2-Chloroethoxy)ethyl methanesulfonate

HRID 2226763

Reaktionsgleichung

Reaktionsgleichung von HRID 2226763
[Cl:1][CH2:2][CH2:3][O:4][CH2:5][CH2:6][OH:7].C(N(CC)CC)C.[CH3:15][S:16](Cl)(=[O:18])=[O:17].O>C1(C)C=CC=CC=1>[S:16]([O:7][CH2:6][CH2:5][O:4][CH2:3][CH2:2][Cl:1])(=[O:18])(=[O:17])[CH3:15]

Komponenten

6

Reaktionsbedingungen

Temperatur
5 °C

Versuchsvorschrift

To a solution of 2-(2-chloroethoxy)ethanol (15.3 g, 123 mmol) in toluene (100 ml) kept at 5° C. was added triethylamine (50 g, 500 mmol). A solution of methanesulfonyl chloride (28 g, 245 mmol) in toluene (50 ml) was carefully added keeping the temperature around 5° C. When addition was complete the reaction mixture was stirred at 5° C. for 45 minutes and then 75 minutes at ambient temperature. Water (100 ml) was added and the mixture was stirred for 15 minutes. The phases were separated and the organic phase was washed with water, brine and dried over magnesium sulphate. The solvent was evaporated in vacuo to give crude 2-(2-chloroethoxy)ethyl mesylate as an oil.

Aufarbeitung

  1. customkept at 5° C.
  2. customthe temperature around 5° C
  3. additionWhen addition
  4. custom75 minutes
  5. customat ambient temperature
  6. stirringthe mixture was stirred for 15 minutes
  7. customThe phases were separated
  8. washthe organic phase was washed with water, brine
  9. dry with materialdried over magnesium sulphate
  10. customThe solvent was evaporated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-109ceabd173a4a51882d63eb6799949d
Quelldatensatz
uspto-grants-1994_09
Patentnummer
US05348965

Verknüpfte Notizen

Wird geladen…