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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101235Generated: November 1, 2026

3,4-dihydro-2H-pyran → 2-(5-Bromopentyloxy)tetrahydro-2H-pyran

https://huagongshe.com/reaction/2101235

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-dihydro-2H-pyranHCID 8080—
Reactant1-Pentanol, 5-bromo-HCID 118709—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Product2-(5-Bromopentyloxy)tetrahydro-2H-pyranHCID 2786933—

Reaction Steps

5-bromopentanol (8 g) was dissolved in dichloromethane (100 mL) and was chilled in an ice bath. Dihydropyran (9 g) was added dropwise followed by p-Toluene sulfonic acid monohydrate (1 g). The mixture was allowed to slowly warm to room temperature and stirred for 18 hours. The mixture was diluted with 200 mL ether, washed with 10% NaOH (100 mL) and dried over MgSO4 to give the title compound. δC (CDCl3, 62.9 MHz): 19.7, 25.0, 25.5, 28.9, 30.7, 32.6, 33.7, 62.4, 67.2 and 89.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572825B2
Source datasetuspto-grants-2009_08
ORD IDord-7083b674d8b14adc818518ac2b28cdd7
Source noteuspto-grants-2009_08