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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6588Generated: October 25, 2026

3,4-dihydro-2H-pyran → 2-(4-Bromobutoxy)tetrahydro-2H-pyran

https://huagongshe.com/reaction/6588

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-dihydro-2H-pyranHCID 8080—
ReactantPotassium CarbonateHCID 11430—
Reactant4-BromobutanolHCID 118388—
SolventDichloromethaneHCID 6344—
SolventPhosphorus oxychlorideHCID 24813—
Product2-(4-Bromobutoxy)tetrahydro-2H-pyranHCID 559019—

Reaction Steps

To a solution of commercially available 4-bromobutan-1-ol (16) (1 equi.) and 3,4-dihydropyran (17) (1.5 equi.) in dichloromethane (3 mL/mmole), phosphorus oxychloride (0.01 equi.) was added at room temperature. The reaction mixture was stirred at that temperature for 24 h. Then potassium carbonate (1 equi.) was added to the reaction mixture and the reaction mixture was stirred at room temperature for 1 h, quenched with water, extracted with dichloromethane, washed with brine, dried over MgSO4, and concentrated in vacuo. Purification by chromatography on silica gel (5% EtOAc (ethylacetate)/hexanes) afforded 2-(4-bromobutoxy) -tetrahydropyran (18), as a colorless oil (88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07083832B2
Source datasetuspto-grants-2006_08
ORD IDord-9c10f800168b48649bfb59f8e3d09d94
Source noteuspto-grants-2006_08