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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284487Generated: October 30, 2026

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

https://huagongshe.com/reaction/2284487

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 numberUS09145429B2
Source datasetuspto-grants-2015_09
ORD IDord-fdc1afb1e35d450b8278ebc7aabcec87
Source noteuspto-grants-2015_09