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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2294240Generated: November 1, 2026

HCID 21474294, compound → HCID 10220846, compound

https://huagongshe.com/reaction/2294240

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 21474294HCID 21474294—
ReactantHCID 21474354HCID 21474354—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
ProductHCID 10220846HCID 10220846—

Reaction Steps

3-Benzyloxy-1-(2-hydroxy-ethyl)-2-(hydroxy-phenyl-methyl)-1H-pyridin-4-one: 3.39 g of 3-benzyloxy-1-(2-hydroxy-ethyl)-2-[phenyl-(tetrahydropyran-2-yloxy)-methyl]-1H-pyridin-4-one are boiled under reflux for 3 hours in 40 ml of ethanol and 10 ml of 2N HCl. For working-up, the ethanol is removed using a rotary evaporator. The residue is diluted with 50 ml of water and covered with 10 ml of ethyl acetate. Then, with stirring, 25 ml of saturated aqueous sodium hydrogen carbonate solution are added. The resulting product is filtered off and washed with water and ethyl acetate. After drying, 3-benzyloxy-1-(2-hydroxy-ethyl)-2-(hydroxy-phenyl-methyl)-1H-pyridin-4-one remains, in the form of colourless crystals. M.p.: 191.5°-192.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05688815
Source datasetuspto-grants-1997_11
ORD IDord-b7ea848edea14faeb67331462debc575
Source noteuspto-grants-1997_11