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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799651Generated: November 1, 2026

3,4-dihydro-2H-pyran → 9-Tetrahydropyranyloxy-1-bromononane

https://huagongshe.com/reaction/1799651

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-dihydro-2H-pyranHCID 8080—
Reactant1-Nonanol, 9-bromo-HCID 108700—
ReactantBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
SolventDichloromethaneHCID 6344—
Product9-Tetrahydropyranyloxy-1-bromononaneHCID 1094672989%

Reaction Steps

A solution of 9-bromo-1-nonanol (2.00 g, 8.96 mmol), 3,4-dihydro-2H-pyran (792 mg, 9.41 mmol), and pyridinium toluene-4-sulfonate (1.08 g, 4.30 mmol) in dichloromethane (34 mL) was stirred at room temperature for 16 h, then washed with 2 M aq. sodium carbonate solution and brine, dried over sodium sulfate, filtered, and evaporated. Chromatography (SiO2; heptane-ethyl acetate gradient) produced 2-(9-bromo-nonyloxy)-tetrahydro-pyran (2.45 g, 89%). Colorless oil, m/e=324.1 ([M+NH4]).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344027B2
Source datasetuspto-grants-2013_01
ORD IDord-a5f071b285554283a3f763467afaf991
Source noteuspto-grants-2013_01