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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013292Generated: November 2, 2026

N-bromobutanimide → Ethyl 3-Bromoindole-2-carboxylate

https://huagongshe.com/reaction/1013292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantEthyl indole-2-carboxylateHCID 73125—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-Bromoindole-2-carboxylateHCID 4715017—

Reaction Steps

To a stirred solution of ethyl 1H-indole-2-carboxylate (9.45 g) in tetrahydrofuran (100 mL) was added N-bromosuccinimide (8.89 g, 50 mmol). The mixture was stirred at room temperature for 1 hour. The mixture was concentrated under vacuum and the residue was dissolved with water (100 ml) and diethyl ether (300 ml). The organic layer was washed with water brine and dried over Na2SO4. After filtration, concentration of solvent afforded the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981888B2
Source datasetuspto-grants-2011_07
ORD IDord-55764f20deef48b9b0933d6d565b73fb
Source noteuspto-grants-2011_07