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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1020803Generated: November 2, 2026

3,4-dihydro-2H-pyran → HCID 86661718, compound

https://huagongshe.com/reaction/1020803

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—
Reactant2-Bromo-5-hydroxybenzaldehydeHCID 387179—
SolventDichloromethaneHCID 6344—
ProductHCID 86661718HCID 8666171820%

Reaction Steps

To a solution of 2-bromo-5-hydroxybenzaldehyde (10 g, 49.75 mmol) and 3,4 dihydro-2H-pyran (4.96 mL, 54.7 mmol) in CH2Cl2 (35 mL) was added camphorsulfonic acid (230 mg, 0.99 mmol), and the mixture 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, 70 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-bromo-5-(tetrahydro-2H-pyran-2-yloxy)benzaldehyde (2.22 g, 20%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716478B2
Source datasetuspto-grants-2014_05
ORD IDord-de6cf937474a482c85062ae6cbfd90af
Source noteuspto-grants-2014_05