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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1870512Generated: November 1, 2026

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

https://huagongshe.com/reaction/1870512

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-dihydro-2H-pyranHCID 8080—
Reactant4-Nitrobenzyl alcoholHCID 69275—
ReactantSodium BicarbonateHCID 516892—
CatalystBicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)-HCID 18462—
SolventEthyl AcetateHCID 8857—
Product2-((4-Nitrobenzyl)oxy)tetrahydro-2H-pyranHCID 1090065596.3%

Reaction Steps

To a solution of 4-nitrobenzylalcohol (50 g, 0.326 mol) in ethyl acetate (EtOAc) (200 ml) were added 3,4-dihydropyran (35.7 ml, 0.392 mol) and CSA (camphor sulfonic acid) (379 mg, 1.63 mmol) under stirring at room temperature, and the mixture was stirred at room temperature for 1 hour. After the reaction completed, the reaction mixture was neutralized with saturated NaHCO3 solution and separated ethyl acetate layer was dried with MgSO4 and concentrated under reduced pressure. The residue was purified with silica gel column chromatography to give 4-(2-tetrahydropyranyloxymethyl)nitrobenzene (74.5 g, 96%) as syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06096780
Source datasetuspto-grants-2000_08
ORD IDord-7c09c45cd4184b3c96a51f9ba3b17ac5
Source noteuspto-grants-2000_08