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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542548Generated: November 1, 2026

3,4-dihydro-2H-pyran → HCID 13672381, compound

https://huagongshe.com/reaction/542548

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-dihydro-2H-pyranHCID 8080—
ReactantBicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)-HCID 18462—
ReactantHCID 13672378HCID 13672378—
SolventDichloromethaneHCID 6344—
ProductHCID 13672381HCID 1367238182.3%

Reaction Steps

In this example, 5 m moles of 4-benzyloxy-2-(11-hydroxyundecyl)-quinoline-N-oxide is dissolved in dichloromethane, and a catalytic amount of D-camphorsulfonic acid and 6 m moles of 2,3-dihydropyran are added thereto. The mixture is stirred at room temperature for 3 hours. Then, the reaction solution is washed with an aqueous sodium hydrogen carbonate solution and then with water, and dried over anhydrous sodium sulfate. The solvent is removed therefrom by distillation, and the residue is purified by silica gel column procedure, whereby the cationed compound is obtained as a colorless oily substance (yield: 82.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04657916
Source datasetuspto-grants-1987_04
ORD IDord-6d5c18019d814f64ad165299acea7441
Source noteuspto-grants-1987_04