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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428004Generated: October 29, 2026

3,4-dihydro-2H-pyran → 2-[(2-Bromophenyl)methoxy]oxane

https://huagongshe.com/reaction/428004

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-dihydro-2H-pyranHCID 8080—
Reactant2-Bromobenzyl alcoholHCID 72850—
ReactantSodium BicarbonateHCID 516892—
CatalystBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
SolventDichloromethaneHCID 6344—
Product2-[(2-Bromophenyl)methoxy]oxaneHCID 531502699.3%

Reaction Steps

Pyridinium p-toluenesulfonate (0.30 g) was added to a solution of 2-bromobenzylalcohol (25.00 g, 0.134 mol) in methylene chloride (100 ml), and the mixture was stirred at room temperature. 3,4-Dihydro-2H-pyran (16.86 g, 0.200 mol) was added thereto. The mixture was stirred at room temperature for 2 hours, and saturated aqueous sodium bicarbonate solution (200 ml) was added. The resulting mixture was extracted with methylene chloride and dried over anhydrous magnesium sulfate. Evaporation of the solvent gave the desired compound 1-bromo-2-(tetrahydropyran-2-yloxymethyl)benzene (36.00 g, 99.3%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313150B1
Source datasetuspto-grants-2001_11
ORD IDord-3f4c753e6db9454fb6153bf8bb0fb11b
Source noteuspto-grants-2001_11