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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 865547Generated: October 30, 2026

3-Allyl-4-hydroxybenzonitrile → 4-hydroxy-3-propylBenzonitrile

https://huagongshe.com/reaction/865547

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Allyl-4-hydroxybenzonitrileHCID 258442—
ReactantEthyl acetate hexaneHCID 21226206—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product4-hydroxy-3-propylBenzonitrileHCID 1398766999.6%

Reaction Steps

A Parr hydrogenation shaker was charged with a solution of 29.76 g (187 mmol) of the product of Step A in 100 mL of ethanol and 3.00 g of a 10% palladium on carbon catalyst was added. The flask was mounted in the hydrogenation appartus, freed of air, pressurized with hydrogen (40 psig) and shaken 80 minutes. At the end of this preiod, TLC analysis (15% ethyl acetate/hexane) indicated that the reaction was complete and the reaction mixture was filtered and evaporated. The product was dried in vacuo to afford 30.01 g (99%) of the title compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05565485
Source datasetuspto-grants-1996_10
ORD IDord-ac7037940627436d94a0c8b14635c28f
Source noteuspto-grants-1996_10