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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378876Generated: October 31, 2026

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

https://huagongshe.com/reaction/1378876

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 apparatus, freed of air, pressurized with hydrogen (40 psig) and shaken 80 minutes. At the end of this period, 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 numberUS05668176
Source datasetuspto-grants-1997_09
ORD IDord-8d81cb0521dd4118b4af26255d8d55cb
Source noteuspto-grants-1997_09