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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342769Generated: October 31, 2026

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

https://huagongshe.com/reaction/342769

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-allyl-5-hydroxy-N-(4-chlorophenyl)indoleHCID 54126383—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product5-hydroxy-4-propyl-N-(4-chlorophenyl)indoleHCID 53747016—

Reaction Steps

4-allyl-5-hydroxy-N-(4-chlorophenyl)indole (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 numberUS05859051
Source datasetuspto-grants-1999_01
ORD IDord-7539911006f84abd9c786bc8d010741f
Source noteuspto-grants-1999_01