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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 466342Erstellt: 24. Oktober 2026

Hydrochloric Acid → 1,3-Bis(2,2-dimethyl-4-pentenoyloxy)-propane

https://huagongshe.com/de/reaction/466342

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt1,3-DibromopropaneHCID 8001—
EduktSodium HydroxideHCID 14798—
Edukt2,2-Dimethyl-4-pentenoic acidHCID 140065—
LösungsmittelWaterHCID 962—
Produkt1,3-Bis(2,2-dimethyl-4-pentenoyloxy)-propaneHCID 1974552668,5%

Reaktionsschritte

To a mixture of 2.6 g (0.02 mole) of 2,2-dimethyl-4-pentenoic acid (XII) and 50 ml of hexamethylphosporic triamide a solution of 1.2 g (0.03 mole) of sodium hydroxide in 3.6 ml of water is added. The reaction mixture is stirred at room temperature for 1 hour and then 1.2 ml (2.4 g, 0.012 mole) of 1,3-dibromopropane are added. The mixture is stirred at room temperature for 4 hours, then poured onto 100 ml of 5% aqueous hydrochloric acid and extracted twice with 50 ml of diethyl ether each. The organic phase is washed twice with 25 ml of water each, dried over sodium sulfate and the solvent is distilled off under reduced pressure. The crude product thus obtained is purified by chromatography on a silica gel column eluted with a 7:3 mixture of hexane and diethyl ether. Thus 2.03 g of the desired compound are obtained in the form of a colourless oil. Yield: 68.5%. According to TLC chromatography using the above-specified eluent Rf =0.6.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05155260
Quelldatensatzuspto-grants-1992_10
ORD IDord-d0e06574e7ca4cc7951fc21f74d5cc03
Quellennotizuspto-grants-1992_10