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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 609725Generated: October 30, 2026

5-Bromoindole → HCID 15326267, compound

https://huagongshe.com/reaction/609725

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-BromoindoleHCID 24905—
ReactantN-MethylmaleimideHCID 70261—
SolventAcetic AcidHCID 176—
ProductHCID 15326267HCID 1532626775%

Reaction Steps

To a solution of 5-bromoindole (5 g, 25.5 mmol) in glacial acetic acid (60 mL) was added N-methylmaleimide (6.1 g, 56.11 mmol) and the resulting mixture was heated to reflux for 4 days. The acetic acid was removed by distillation and the crude product was dissolved in diethyl ether (500 mL) and washed with saturated sodium bicarbonate (2×100 mL) and brine (3×100 mL). The solvent was evaporated and the residue chromatographed on silica gel using hexane/ethyl acetate (1:1) as the eluent to provide 3-(5-bromo-1H-indol-3-yl)-N-methylsuccinimide (5.85 g, 75%) which was used directly for the next reaction. Yellow solid, mp 194-195° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05998438
Source datasetuspto-grants-1999_12
ORD IDord-f82a08e58c4d4941b240db4c8d16bff5
Source noteuspto-grants-1999_12