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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421156Generated: November 1, 2026

Indole → HCID 18780221, compound

https://huagongshe.com/reaction/1421156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
ReactantHCID 18780241HCID 18780241—
ReactantHCID 178418373HCID 178418373—
SolventBenzeneHCID 241—
SolventDiethyl EtherHCID 3283—
ProductHCID 18780221HCID 187802210.9%

Reaction Steps

1.4 ml of a 3M solution of methylmagnesium iodide in diethyl ether was added to a solution of 360 mg indole in 20 ml of benzene under nitrogen. After stirring at room temperature for 10 minutes 300 mg of 3-bromo-4-(4-nitrophenyl)-1H-pyrrole-2,5-dione were added and the resulting mixture was heated to reflux for 4 days. After cooling the solution was evaporated and the residue was partitioned between dichloromethane and 2M hydrochloric acid. The organic phase was washed with water, dried and evaporated. The residue was purified on silica gel with dichloromethane and 1% methanol in dichloromethane and then with 20% methanol/water on Hypersil to give 3 mg of 3-(3-indolyl)-4-(4-nitrophenyl)-1H-pyrrole-2,5-dione, m.p. 125° C. (decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE036736
Source datasetuspto-grants-2000_06
ORD IDord-1ab53b350e164f1aa7300d05932bcf22
Source noteuspto-grants-2000_06