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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1392762Generated: November 4, 2026

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

https://huagongshe.com/reaction/1392762

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 numberUS07342014B2
Source datasetuspto-grants-2008_03
ORD IDord-085e8f43dfa8450798e34e7a06b28371
Source noteuspto-grants-2008_03