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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 258923Erstellt: 24. Oktober 2026

3,4-dihydro-2H-pyran → 2-(p-Bromo-alpha-methylbenzyloxy)tetrahydropyran

https://huagongshe.com/de/reaction/258923

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3,4-dihydro-2H-pyranHCID 8080—
Edukt1-(4-Bromophenyl)ethanolHCID 95352—
KatalysatorHydrochloric AcidHCID 313—
LösungsmittelDiethyl EtherHCID 3283—
Produkt2-(p-Bromo-alpha-methylbenzyloxy)tetrahydropyranHCID 11219861—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A mixture of 269 parts of p-bromo-α-methylbenzyl alcohol and 225 parts of 2H-3,4-dihydropyran is stirred and cooled to 0° C. Then there are added dropwise 10 drops of concentrated hydrochloric acid solution and the whole is stirred in an ice-bath (room temperature is reached). After stirring for 24 hours, the reaction mixture is poured onto 1200 parts of ether. The organic phase is washed twice with a sodium hydrogen carbonate solution and twice with water, dried, filtered and evaporated. The residue is distilled, yielding 2-(p-bromo-α-methylbenzyloxy)tetrahydropyran; bp. 165°-177° C. at 20 mm. pressure.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04035376
Quelldatensatzuspto-grants-1977_07
ORD IDord-7de4891e22fe41ca84d1bd5bba4b0925
Quellennotizuspto-grants-1977_07