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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982005Generated: October 29, 2026

5-Bromoindole → 2-(1H-Indol-5-yl)-N,N-dimethylethenesulphonamide

https://huagongshe.com/reaction/982005

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-BromoindoleHCID 24905—
ReactantTri-o-tolylphosphineHCID 80271—
ReactantN,N-dimethylethene-1-sulfonamideHCID 19037148—
Catalystpalladium(II) acetateHCID 167845—
SolventAcetonitrileHCID 6342—
Product2-(1H-Indol-5-yl)-N,N-dimethylethenesulphonamideHCID 5417150338.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 5-bromoindole (7.7 g), N,N-dimethylethenesulphonamide (5.3 g) triethylamine (15 ml), acetonitrile (5 ml), palladium (II) acetate (0.35 g) and tri-o-tolylphosphine (0.95 g) was heated at 100° C. in an autoclave for 3 h. The resulting cooled mixture was partitioned between hydrochloric acid (2N, 300 ml) and ethyl acetate (2×150 ml). The combined extracts were dried (Na2SO4) and evaporated in vacuo. The residue was purified by `flash` chromatography (V, 7 cm col.) to give the title compound as a crystalline solid (3.8 g) m.p. 148°-150° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04994483
Source datasetuspto-grants-1991_02
ORD IDord-d0ff7951d44f4785957f6658ff277433
Source noteuspto-grants-1991_02