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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 358312Erstellt: 24. Oktober 2026

Epichlorohydrin → Isostearyl glycidyl ether

https://huagongshe.com/de/reaction/358312

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEpichlorohydrinHCID 7835—
EduktSodium HydroxideHCID 14798—
EduktIsostearyl Alcohol EXHCID 62825—
KatalysatorStearyltrimethylammonium chlorideHCID 8155—
LösungsmittelHexaneHCID 8058—
ProduktIsostearyl glycidyl etherHCID 2262280483,2%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

Into a round bottom flask having a capacity of 1 liter and equipped with a reflux condenser, a thermometer, a dropping funnel, and a stirring means, 120 g of a 50% sodium hydroxide solution (60 g (1.5 mole) as pure sodium hydroxide), 68 g (0.25 mole) of isostearyl alcohol [5,7,7-trimethyl-2-(1,3,3-trimethylbutyl) octanol], 200 ml of n-hexane, and 2.51 g (0.0075 mole) of stearyl trimethyl ammonium chloride, were introduced in this order. The reaction mixture was kept at a reaction temperature of 25° C. in a water bath, and while vigorously stirring the mixture at a stirring speed of 400 r.p.m., 93 g (1 mole) of epichlorohydrin was added dropwise from the dropping funnel. It took about 1.5 hours for the addition of the epichlorohydrin, and the reaction mixture was heated to 50° C. and stirred for about 8 hours at this temperature. After the completion of the reaction, the mixture was treated in a usual manner, whereupon 67.9 g (yield: 83%) of isostearyl glycidyl ether (5,7,7-trimethyl-2-(1,3,3-trimethylbutyl)-octyl glycidyl ether) was obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04465869
Quelldatensatzuspto-grants-1984_08
ORD IDord-f627163b3e1b4da8aeca592dd6510e85
Quellennotizuspto-grants-1984_08