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Water → HCID 11076628, Verbindung

HRID 1792313
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1792313
[CH3:1][O:2][CH2:3][CH2:4][O:5][CH2:6][CH2:7][OH:8].[C:9]1([CH3:19])[CH:14]=[CH:13][C:12]([S:15](Cl)(=[O:17])=[O:16])=[CH:11][CH:10]=1.O>N1C=CC=CC=1>[C:9]1([CH3:19])[CH:14]=[CH:13][C:12]([S:15]([O:8][CH2:7][CH2:6][O:5][CH2:4][CH2:3][O:2][CH3:1])(=[O:17])=[O:16])=[CH:11][CH:10]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 962WaterHCID 73974-Toluenesulfonyl chlorideHCID 8134Diethylene Glycol Monomethyl Ether

Produkt 1

HCID 11076628HCID 11076628, VerbindungAusbeute 98,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1049PyridineLösungsmittel

Versuchsvorschrift

To a solution of diethylene glycol monomethylether (12 g, 100 mmol) in pyridine (70 ml) was added p-toluenesulfonyl chloride (22.8 g, 120 mmol) at 0° C., which was then stirred at room temperature for 2 hours. Water was added thereto, and the mixture was extracted with diethyl ether. The extracted organic layer was washed with 0.5N-HCl, water and saturated sodium bicarbonate solution, and dried over anhydrous magnesium sulfate. The organic solvent was removed under reduced pressure to give the title compound (27 g, stoichiometric yield) as a yellow oil. The compound thus obtained was used in the next reaction without further purification.

Aufarbeitung

  1. extractionthe mixture was extracted with diethyl ether
  2. washThe extracted organic layer was washed with 0.5N-HCl, water and saturated sodium bicarbonate solution
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customThe organic solvent was removed under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-8c8a90937fc941d6aa4e1f527bfdf07d
Quelldatensatz
uspto-grants-2006_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07074819B2

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