HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → Ethyl 3-bromo-5-chloro-1H-indole-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Ethyl 5-chloroindole-2-carboxylate | HCID 78518 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 3-bromo-5-chloro-1H-indole-2-carboxylate | HCID 13466333 | 100.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07365205B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-f572e1e6ee054bc7b7ce542075dceae4 |
| Source note | uspto-grants-2008_04 |