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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418454Generated: November 3, 2026

ethyl 4-(3-benzyloxy-5-fluorophenyl)-3,4,5,6-tetrahydro-2H-pyran-4-carboxylate → 4-(3-Fluoro-5-hydroxyphenyl)-3,4,5,6-tetrahydro-2H-pyran-4-carboxylate Ethyl

https://huagongshe.com/reaction/1418454

Reaction equation

Participants

RoleNameHCIDCharge
Reactantethyl 4-(3-benzyloxy-5-fluorophenyl)-3,4,5,6-tetrahydro-2H-pyran-4-carboxylateHCID 18786326—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product4-(3-Fluoro-5-hydroxyphenyl)-3,4,5,6-tetrahydro-2H-pyran-4-carboxylate EthylHCID 1878637499.9%

Reaction Steps

A mixture of ethyl 4-[3-(benzyloxy)-5-fluorophenyl]-3,4,5,6-tetrahydro-2H-pyran-4-carboxylate (2.70 g, 7.5 mmol) and 10% palladium on activated carbon (0.27 g) in ethanol (100 ml) was stirred under a hydrogen atmosphere for 3.25 hr. Catalyst was removed by filtration and evaporation of the filtrate gave the titled compound as a colorless liquid (2.01 g, quantitative yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05883106
Source datasetuspto-grants-1999_03
ORD IDord-aef9c3e9b5c94ca5a67db092051347fc
Source noteuspto-grants-1999_03