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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284482Generated: October 30, 2026

3,4-dihydro-2H-pyran → HCID 59838331, compound

https://huagongshe.com/reaction/2284482

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-dihydro-2H-pyranHCID 8080—
Reactant4-Bromo-3,5-dimethylphenolHCID 81970—
CatalystBicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)-HCID 18462—
SolventDichloromethaneHCID 6344—
ProductHCID 59838331HCID 59838331362.9%

Reaction Steps

A mixture of 4-bromo-3,5-dimethylphenol (4.6 g, 22.88 mmol), 3,4 dihydro-2H-pyran (2.69 mL, 29.7 mmol) in 8.0 mL of CH2Cl2, and camphorsulfonic acid (106 mg, 4.56 mmol) was stirred at room temperature for 21 h. The reaction mixture was then quenched with equal volumes of 0.2 M NaOH and EtOAc (1:1, 20 mL) before the layers were separated. The water phase was further extracted with equal volume of EtOAc before the organic layers were combined and dried over anhydrous Na2SO4 and filtered. The solvent was removed under reduced pressure. The residue was purified by silica gel column using Combiflash to give 2-(4-bromo-3,5-dimethylphenoxy)tetrahydro-2H-pyran (23.68 g, 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145429B2
Source datasetuspto-grants-2015_09
ORD IDord-57dfa736db1a4b299b57e8b5bff93111
Source noteuspto-grants-2015_09