Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258923Generated: October 26, 2026

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

https://huagongshe.com/reaction/258923

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-dihydro-2H-pyranHCID 8080—
Reactant1-(4-Bromophenyl)ethanolHCID 95352—
CatalystHydrochloric AcidHCID 313—
SolventDiethyl EtherHCID 3283—
Product2-(p-Bromo-alpha-methylbenzyloxy)tetrahydropyranHCID 11219861—

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04035376
Source datasetuspto-grants-1977_07
ORD IDord-7de4891e22fe41ca84d1bd5bba4b0925
Source noteuspto-grants-1977_07