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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345668Generated: October 30, 2026

Indole → HCID 14855724, compound

https://huagongshe.com/reaction/345668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
ReactantHCID 18780286HCID 18780286—
ReactantHCID 178418573HCID 178418573—
SolventBenzeneHCID 241—
SolventDiethyl EtherHCID 3283—
ProductHCID 14855724HCID 148557242.7%

Reaction Steps

To a suspension of 105 mg of indole in 20 ml of benzene were added 0.6 ml of a 3M solution of methylmagnesium bromide in diethyl ether under nitrogen. The mixture was stirred for 0.5 hour. 100 mg of 3-bromo-4-(5-methoxy-3-indolyl)-1H-pyrrole-2,5-dione were added and the mixture was heated to reflux for 5 days. After cooling the residue was partitioned between dichloromethane and 2M hydrochloric acid. The organic extracts were washed with water, dried and evaporated. The residue was purified on silica gel with 1% methanol in dichloromethane and then with 50% methanol/0.1% trifluoroacetic acid/water on Spherisorb to give 3 mg of 3-(3-indolyl)-4-(5-methoxy-3-indolyl)-1H-pyrrole-2,5-dione, m.p. 280° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05057614
Source datasetuspto-grants-1991_10
ORD IDord-29cb33cab90848fba678c81134a87cfb
Source noteuspto-grants-1991_10