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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342774Generated: October 31, 2026

4-allyl-5-hydroxy-N-(4-fluorobenzyl)indole → 4-propyl-5-hydroxy-N-(4-fluorobenzyl)indole

https://huagongshe.com/reaction/342774

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-allyl-5-hydroxy-N-(4-fluorobenzyl)indoleHCID 53978806—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product4-propyl-5-hydroxy-N-(4-fluorobenzyl)indoleHCID 53701199—

Reaction Steps

4-allyl-5-hydroxy-N-(4-fluorobenzyl)indole (Step C; 0.40 g, 1.42 mmol) was taken up in 10 mL ethyl acetate and hydrogenated (1 atm) at ambient temperature using 5% palladium on charcoal (15 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 numberUS05859051
Source datasetuspto-grants-1999_01
ORD IDord-9aff132308f947809bee9000b430f7ab
Source noteuspto-grants-1999_01