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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322984Generated: October 30, 2026

Hydrochloric Acid → 6-(2-Methylphenyl)-tetrahydropyran-2-one

https://huagongshe.com/reaction/322984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
Reactant5-(2-Methylphenyl)-5-oxovaleric acidHCID 2760003—
ReactantSodium borohydrideHCID 4311764—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product6-(2-Methylphenyl)-tetrahydropyran-2-oneHCID 2201026057.1%

Reaction Steps

To a stirred suspension of 5-oxo-5-(2-methylphenyl)pentanoic acid (10 g) in water (100 mL) is added potassium hydroxide pellets (6.35 g). The temperature of the mixture is maintained at 2-20° C. whilst sodium borohydride (1.47 g) is added over 15 minutes. The reaction mixture is left at room temperature for 18 hours when 1 N hydrochloric acid (100 mL) is cautiously added followed by water (50 mL) and ethyl acetate (100 mL). The organic phase is separated and the aqueous phase extracted twice with ethyl acetate (100 mL). The combined organic phases are washed with brine (100 mL), dried over magnesium sulphate and evaporated to give 6-(2-methylphenyl)-tetrahydropyran-2-one (5.27 g) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211234B1
Source datasetuspto-grants-2001_04
ORD IDord-749333699eed48ccbc5c23500853bba6
Source noteuspto-grants-2001_04