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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288892Generated: October 30, 2026

4-allyl-5-hydroxy-N-neopentylindole → 5-hydroxy-4-propyl-N-neopentylindole

https://huagongshe.com/reaction/2288892

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-allyl-5-hydroxy-N-neopentylindoleHCID 18672464—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product5-hydroxy-4-propyl-N-neopentylindoleHCID 18672475—

Reaction Steps

4-Allyl-5-hydroxy-N-neopentylindole (Step C; 1.0 g, 3.54 mmol) was taken up in 25 mL ethyl acetate and hydrogenated (1 atm) at ambient temperature using 5% palladium on charcoal (40 mg) for 2 hours. The reaction was filtered through celite and concentrated in vacuo to provide the title compound which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090839
Source datasetuspto-grants-2000_07
ORD IDord-5e8358747000442a9ea104bf9d9e55c1
Source noteuspto-grants-2000_07