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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473054Generated: October 26, 2026

Triethylamine → (E)-5-(2-(phenylsulfonyl)vinyl)-1H-indole

https://huagongshe.com/reaction/473054

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant5-BromoindoleHCID 24905—
ReactantPhenyl vinyl sulfoneHCID 79664—
ReactantTri-o-tolylphosphineHCID 80271—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product(E)-5-(2-(phenylsulfonyl)vinyl)-1H-indoleHCID 1552156085%

Reaction Steps

A solution of 5-bromoindole (5.0 g, 25.5 mmol), phenylvinylsulfone (7.50 g, 44.64 mmol), Pd(OAc)2 (0.46 g, 2.05 mmol), tri-O-tolylphosphine (1.55 g, 5.10 mmol) and triethylamine (4.88 g, 48.46 mmol) was heated to 95-105° C. for 6-15 h in DMF. The reaction mixture was cooled to RT, diluted with dichloromethane and filtered over a bed of filter aid. The filtrate was sequentially washed with water and brine, and dried over sodium sulphate. The organic layer was concentrated under vacuum and the product precipitated from dichloromethane and hexane as a solid in about 85-90% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633239B2
Source datasetuspto-grants-2014_01
ORD IDord-6becbcf7f69841c2875688099706b4fb
Source noteuspto-grants-2014_01