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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116503Generated: October 30, 2026

HCID 178436444, compound → HCID 178436189, compound

https://huagongshe.com/reaction/2116503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178436444HCID 178436444—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
ProductHCID 178436189HCID 17843618983%

Reaction Steps

Next, a mixture of 3-(4-ethylbenzoyl)-4-hydroxypyridine (2.69 g, 0.0118 mol), 20% palladium hydroxide/carbon (530 mg) and methanol (60 mL) was stirred under a hydrogen atmosphere for 18 hours. Additional 20% palladium hydroxide/carbon (300 mg) was added and stirred for 6 hours, followed by further addition of 20% palladium hydroxide/carbon (340 mg) and stirring for 15 hours. After filtration to remove the insoluble materials, the filtrate was purified by silica gel column chromatography (chloroform:methanol=10:1) to give 3-(4-ethylbenzyl)-4-hydroxypyridine (2.09 g, 83%) as a colorless amorphous substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07439232B2
Source datasetuspto-grants-2008_10
ORD IDord-97231aaffe714603a02fa8883528ca1c
Source noteuspto-grants-2008_10