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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 617402Generated: October 30, 2026

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

https://huagongshe.com/reaction/617402

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-yloxy-methyl)benzene (36.00 g, 99.3%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05948819
Source datasetuspto-grants-1999_09
ORD IDord-699808305f7049ddbe0bb5c901df6342
Source noteuspto-grants-1999_09