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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532456Generated: October 26, 2026

Triethylamine → 5-[2-(Phenylsulfonyl)ethenyl]indole

https://huagongshe.com/reaction/1532456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant5-BromoindoleHCID 24905—
Reactant2-(Phenylsulfonyl)ethanolHCID 30202—
ReactantTri-o-tolylphosphineHCID 80271—
ReactantMethanesulfonic anhydrideHCID 81560—
Catalystpalladium(II) acetateHCID 167845—
SolventAcetonitrileHCID 6342—
Product5-[2-(Phenylsulfonyl)ethenyl]indoleHCID 5432856023.3%

Reaction Conditions

Temperature50 °C

Reaction Steps

To 0.186 g (1.0 mmol) of 2-(phenylsulfonyl)ethanol, 3 ml of acetonitrile was added, followed by 0.19 g(1.1 mmol) of methanesulfonic anhydride and 0.56 ml (4.0 mmol) of triethylamine, and the mixture was stirred for 5 hours at an internal temperature of 50° C. Subsequently, 0.29 g (1.5 mmol) of 5-bromoindole, 0.011 g (0.05 mmol) of palladium acetate, and 0.067 g (0.22 mmol) of tri(o-tolyl)phosphine were added, and the mixture was then refluxed for 17 hours. After cooled to room temperature, the reaction mixture was concentrated and purified by column chromatography (hexane/ethyl acetate=70/30) to obtain 0.066 g of 5-[2-(phenylsulfonyl)ethenyl]indole. Yield: 23%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06201131B1
Source datasetuspto-grants-2001_03
ORD IDord-90fb7022e82a4cb485d643bf37510e97
Source noteuspto-grants-2001_03