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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257393Generated: November 2, 2026

3,4-dihydro-2H-pyran → HCID 66939482, compound

https://huagongshe.com/reaction/1257393

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-dihydro-2H-pyranHCID 8080—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 56706473HCID 56706473—
CatalystSulfuric AcidHCID 1118—
SolventTolueneHCID 1140—
ProductHCID 66939482HCID 6693948299.2%

Reaction Steps

To a solution (50 mL) of the compound (7.0 g, 27 mmol) obtained in Example 64b in toluene were added dihydropyran (4.9 mL, 54 mmol) and conc. sulfuric acid (3 drops), and the mixture was stirred at room temperature overnight. The reaction mixture was neutralized with saturated aqueous sodium hydrogen carbonate, and the mixture was extracted with ethyl acetate. The obtained organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The resulting crude title compound was purified by column chromatography (hexane-hexane/ethyl acetate=80/20) to give the title compound (9.2 g, 99%) as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461348B2
Source datasetuspto-grants-2013_06
ORD IDord-27c032fb96394b2d8c200def65e3c00f
Source noteuspto-grants-2013_06