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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756014Generated: October 26, 2026

p-Toluenesulfonic acid → 2-(4-bromophenethoxy)tetrahydro-2H-pyran

https://huagongshe.com/reaction/1756014

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant3,4-dihydro-2H-pyranHCID 8080—
Reactant2-(4-Bromophenyl)ethanolHCID 72851—
ReactantSodium BicarbonateHCID 516892—
SolventDichloromethaneHCID 6344—
Product2-(4-bromophenethoxy)tetrahydro-2H-pyranHCID 13306758—

Reaction Steps

p-Toluenesulfonic acid (0.30 g) was added to a solution of 4-bromophenethyl alcohol (9.50 g, 47.24 mmol) in methylene chloride (50 ml), and the mixture was stirred under ice-cooling. To the mixture was added 3,4-dihydropyran (5.53 g, 65.74 mmol). After stirring under ice-cooling for 20 minutes, a saturated aqueous solution of sodium bicarbonate (40 ml) was added to the reaction mixture. The resulting mixture was extracted with methylene chloride and dried over magnesium sulfate. After evaporation of the solvent, the desired 4-(2-(tetrahydropyran-2-yloxy)ethyl)bromobenzene was obtained (13.40 g, 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05439911
Source datasetuspto-grants-1995_08
ORD IDord-a241b5a3077a404986abd9470ed4b4db
Source noteuspto-grants-1995_08