Hydrochloric Acid → HCID 76456682, Verbindung
Reaktionsgleichung
[CH2:1]([O:4][CH:5]([CH3:8])[CH2:6][OH:7])[CH2:2][CH3:3].[C:9]1([CH3:19])[CH:14]=[CH:13][C:12]([S:15](Cl)(=[O:17])=[O:16])=[CH:11][CH:10]=1.[OH-].[Na+].Cl>C1C=CC=CC=1>[CH2:1]([O:4][CH:5]([CH3:8])[CH2:6][O:7][S:15]([C:12]1[CH:13]=[CH:14][C:9]([CH3:19])=[CH:10][CH:11]=1)(=[O:17])=[O:16])[CH2:2][CH3:3]Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
4.75 g of 2-propoxypropanol, 5.39 g of p-toluenesulfonyl chloride, 2,24 g and 10 ml of benzene were placed in a 50 ml-reaction vessel and stirred in a nitrogen gas stream for 22 hours at room temperature. Thereafter, 8.6 ml of heated conc. NaOH solution was added to the reaction mixture, followed by stirring for 5 minutes. The reaction liquid was poured into 200 ml of cooled 10%-hydrochloric acid solution and extracted with hexane to obtain 3.2 g of 2-propoxypropyl-p-toluenesulfonate (tosylate).
Aufarbeitung
- stirringby stirring for 5 minutes
- customThe reaction liquid
- extractionextracted with hexane
Quellen und Nachweise
- ORD-Eintrag
- ord-e5bcf1f3e33b44aa9f5e01f2382b36b2
- Quelldatensatz
- uspto-grants-1995_12
- Patentnummer
- US05478495
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