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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1857809Generated: October 31, 2026

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

https://huagongshe.com/reaction/1857809

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, 0.0012 mol) was added to a solution of 2-bromobenzyl alcohol (25 g, 0.134 mol) in dichloromethane (100 ml), and the mixture was stirred at room temperature. To this mixture was added 3,4-dihydro-2H-pyrane (16.86 g, 0.20 mol). After the resulting mixture was stirred at room temperature for 2 hours, a saturated aqueous solution (200 ml) of sodium bicarbonate was added. The mixture was extracted with dichloromethane (200 ml). After the mixture was dried over anhydrous magnesium sulfate, the solvent was evaporated to obtain the desired compound 1-bromo-2-(2-tetrahydropyranyloxymethyl)benzene (36.00 g, Yield: 99.3%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06147231
Source datasetuspto-grants-2000_11
ORD IDord-5fb9b1a9a6f64a6cb86967c5dce4bb4b
Source noteuspto-grants-2000_11