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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1194832Erstellt: 27. Oktober 2026

Butyl 3-(p-tert-butylphenoxy)-propionate → 3-p-t-Butyl-phenoxypropanol

https://huagongshe.com/reaction/1194832

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktButyl 3-(p-tert-butylphenoxy)-propionateHCID 14423333—
EduktAluminium lithium hydrideHCID 21226445—
LösungsmittelDiethyl EtherHCID 3283—
Produkt3-p-t-Butyl-phenoxypropanolHCID 13313735—

Reaktionsbedingungen

Temperatur-5 °C

Reaktionsschritte

This ester 21.0 g was dissolved in 500 ml dry ether and cooled to -5° C. in an ice/acetone bath. To the cold solution was added, cautiously, a slurry of 3.5 g lithium aluminum hydride in 100 ml dry ether. After one hour the excess lithium aluminum hydride was destroyed by the cautious addition of 200 ml ethyl acetate, then 50 ml water. The solution was filtered and the filtrate partitioned between 200 ml ether-200 ml water. The organic layer was removed, dried, and evaporated to a yellow oil which was vacuum distilled (116° C./0.35 mm) over potassium carbonate to a clear colorless oil, 3-p-t-butylphenoxypropanol, 10.1 g (64%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04816491
Quelldatensatzuspto-grants-1989_03
ORD IDord-ecbfde36926647cf954d8fa5ef59a520
Quellennotizuspto-grants-1989_03