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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366517Generated: October 31, 2026

Toluene → 5-[4-(4-Benzyl-piperidin-1-yl)-but-1-ynyl]-1H-indole

https://huagongshe.com/reaction/366517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantBenzenesulfonyl chlorideHCID 7369—
Reactant5-BromoindoleHCID 24905—
Reactant1-(Benzenesulfonyl)-5-bromo-1H-indoleHCID 2776210—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventWaterHCID 962—
SolventSodium HydroxideHCID 14798—
Product5-[4-(4-Benzyl-piperidin-1-yl)-but-1-ynyl]-1H-indoleHCID 10641073—

Reaction Steps

1-Benzenesulfonyl-5-bromoindole. A mixture of 5-bromoindole (5 g, 25.5 mmol) and tetra-n-butylammonium hydrogen sulfate (866 mg, 2.55 mmol) in 50% NaOH (50 mL) and toluene (200 mL) is stirred at room temperature for 5 min. Benzenesulfonyl chloride (3.57 mL, 28 mmol) is added and the mixture stirred for 1 hr. The mixture is diluted with water (500 mL) and extracted with EtOAc (3×100 mL). The extracts are washed with brine (250 mL), dried over MgSO4, filtered and evaporated to a yellow oil. The oil is purified by medium-pressure column chromatography on silica gel eluting with 10% EtOAc/hexanes to give the title compound as a white solid (7.81 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06130234
Source datasetuspto-grants-2000_10
ORD IDord-fd3c74e9053c4d6b856d6c9a3df5f433
Source noteuspto-grants-2000_10