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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836558Generated: October 31, 2026

Ethyl(4-{4-(benzyloxy)-3-[(4-fluorophenyl)sulphonyl]benzyl}-3,5-dimethylphenoxy)acetate → Ethyl (4-{3-[(4-fluorophenyl)sulphonyl]-4-hydroxybenzyl}-3,5-dimethylphenoxy)acetate

https://huagongshe.com/reaction/1836558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl(4-{4-(benzyloxy)-3-[(4-fluorophenyl)sulphonyl]benzyl}-3,5-dimethylphenoxy)acetateHCID 23499607—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductEthyl (4-{3-[(4-fluorophenyl)sulphonyl]-4-hydroxybenzyl}-3,5-dimethylphenoxy)acetateHCID 86588309—

Reaction Steps

50 mg (0.09 mmol) of ethyl (4-{4-(benzyloxy)-3-[(4-fluorophenyl)sulphonyl]benzyl}-3,5-dimethylphenoxy)acetate (Example XI) are dissolved in 20 ml of ethanol. 10 mg of palladium on activated carbon (10%) are added, and the mixture is hydrogenated at 1013 mbar and room temperature for 2 hours. The reaction mixture is then filtered through Celite and the solvent is removed under reduced pressure. This gives 37 mg (86% of theory) of ethyl (4-{3-[(4-fluorophenyl)sulphonyl]-4-hydroxybenzyl}-3,5-di-methylphenoxy)acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06777442B2
Source datasetuspto-grants-2004_08
ORD IDord-7d5048432f1942babfb1d6b99c2178f9
Source noteuspto-grants-2004_08