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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004380Generated: October 30, 2026

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

https://huagongshe.com/reaction/1004380

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-bromobenzylalcohol (25 g, 0.134 mol) in dichloromethane (100 ml), and the mixture was stirred at room temperature. 3,4-Dihydro-2H-pyran (16.86 g, 0.20 mol) was added thereto. The mixture was stirred at room temperature for 2 hours. Then, saturated aqueous sodium bicarbonate solution (200 ml) was added, and the mixture was extracted with dichloromethane (200 ml). After drying over anhydrous magnesium sulfate, the solvent was evaporated to give the desired 1-bromo-2-(2-tetrahydropyranyloxymethyl)benzene (36.00 g, yield: 99.3%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06048885
Source datasetuspto-grants-2000_04
ORD IDord-d13973fbabbc4d11b3bc136c0e8db830
Source noteuspto-grants-2000_04