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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902868Generated: October 27, 2026

N-bromobutanimide → Ethyl 3-bromo-5-chloro-1H-indole-2-carboxylate

https://huagongshe.com/reaction/902868

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantEthyl 5-chloroindole-2-carboxylateHCID 78518—
SolventDimethylformamideHCID 6228—
ProductEthyl 3-bromo-5-chloro-1H-indole-2-carboxylateHCID 13466333100.5%

Reaction Steps

N-Bromosuccinimide (440 mg) was added to a solution of ethyl 5-chloroindole-2-carboxylate (500 mg) in N,N-dimethylformamide (10 ml). The reaction mixture was stirred at room temperature for 18 hours, and the solvent was distilled off under reduced pressure. The residue was partitioned in ethyl acetate and water, and a water layer was extracted with ethyl acetate. The resultant organic layers were combined, washed with saturated aqueous solution of sodium chloride and then dried over anhydrous sodium sulfate. The solvent was distilled off, the residue was purified by column chromatography on silica gel (ethyl acetate:hexane=1:9), and white powder thus obtained was washed with hexane to obtain the title compound (680 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07365205B2
Source datasetuspto-grants-2008_04
ORD IDord-f572e1e6ee054bc7b7ce542075dceae4
Source noteuspto-grants-2008_04