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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254171Generated: October 27, 2026

Hydrochloric Acid → 4-(3-Benzyloxyphenyl)-4-hydroxy-2,6-dimethyltetrahydropyran

https://huagongshe.com/reaction/2254171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
Reactant1-(Benzyloxy)-3-bromobenzeneHCID 2756638—
ReactantMagnesiumHCID 5462224—
ReactantHCID 178419633HCID 178419633—
Product4-(3-Benzyloxyphenyl)-4-hydroxy-2,6-dimethyltetrahydropyranHCID 20080604—

Reaction Steps

A solution of 2,60dimethyltetrahydropyran-4-one (2.2 g) in tetrahydrofuran (5 ml) was added to a solution of 3-benzyloxyphenylmagnesium bromide [prepared by heating a mixture of 3-benzyloxybromobenzene (5 g), magnesium (0.5 g) and tetrahydrofuran (20 ml)] in tetrahydrofuran and the mixture was stirred at ambient temperature for 3 hours. The mixture was cooled to 5° C., ice (5 ml) and 2N hydrochloric acid solution (25 ml) were added, and the mixture was extracted with ethyl acetate. The organic phase was washed with a saturated sodium chloride solution, dried (MgSO4) and evaporated. The residue was purified by column chromatography using increasingly polar mixtures of toluene and ethyl acetate as eluent. There were thus obtained two isomers of 4-(3-benzyloxyphenyl)-4-hydroxy-2,6-dimethyltetrahydropyran: a less polar isomer (2.41 g, 45%),

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05234950
Source datasetuspto-grants-1993_08
ORD IDord-72bcb042682146bc8cb8b20e6da6c359
Source noteuspto-grants-1993_08