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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982009Generated: October 26, 2026

Triethylamine → 2-(1H-indol-5-yl)-N-methylethenesulfonamide

https://huagongshe.com/reaction/982009

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant5-BromoindoleHCID 24905—
ReactantN-MethylethenesulfonamideHCID 21895383—
CatalystTri-o-tolylphosphineHCID 80271—
SolventAcetonitrileHCID 6342—
Product2-(1H-indol-5-yl)-N-methylethenesulfonamideHCID 1347576428.9%

Reaction Steps

A mixture of 5-bromoindole (6.6 g), N-methylethenesulphonamide (5.1 g) palladium (II) acetate (75 mg), tri-o-tolylphosphine (0.2 g), triethylamine (12 ml), and acetonitrile (5 ml) was heated at 100° in an autoclave for 3 h. The reaction mixture was cooled and partitioned between hydrochloric acid (1N, 300 ml) and ethyl acetate (2×150 ml). The combined extracts were dried, (Na2SO4) and evaporated in vacuo to give an oil which was purified by `flash` chromatography (Q, 7 cm dia. col.) to give the title compound as a solid (2.3 g) m.p. 164√-166°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04994483
Source datasetuspto-grants-1991_02
ORD IDord-dbdd133000904a6aa455d06e7c3ac5a1
Source noteuspto-grants-1991_02