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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1045335Erstellt: 25. Oktober 2026

Sodium Hydroxide → HCID 58264321, Verbindung

https://huagongshe.com/reaction/1045335

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
EduktGlyceryl Allyl EtherHCID 78950—
EduktLinoleyl methanesulfonateHCID 59753235—
KatalysatorTetrabutylammonium hydrogen sulfateHCID 94433—
LösungsmittelTolueneHCID 1140—
ProduktHCID 58264321HCID 58264321—

Reaktionsbedingungen

Temperatur2.5 °C

Reaktionsschritte

In a 2000 mL round bottom flask equipped with a large magnetic stir bar, 3-allyloxypropane-1,2-diol (5.94 g, 45 mmol), and tetrabutylammonium hydrogen sulfate (6 g, 18 mmol) were added. A solution of linoleyl mesylate (33.8 g, 98 mmol) in toluene (150 mL) was also made and added. The mixture was cooled to 0-5° C. with an ice bath. 50% sodium hydroxide (70 mL) was then slowly added, rinsing in with deionized water (20 mL). The resulting mixture is stirred at room temperature, under nitrogen for 40 hours. Deionized water (200 mL) and isopropyl acetate (200 mL) were added and the mixture stirred vigorously for a further 10-15 min. The mixture was transferred to a 1000-mL separating funnel and allowed to separate. The aqueous phase was removed and the organic phase washed with saturated sodium chloride solution (2×150 mL). The organic phase was dried with magnesium sulfate (40 g), filtered, and concentrated to obtain a neat orange oil. The oil was purified by column chromatography. Final yield: 19.5 g (69%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08569256B2
Quelldatensatzuspto-grants-2013_10
ORD IDord-afd5f79a56104055a1a2250e6860e35d
Quellennotizuspto-grants-2013_10