HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Ethyl Ketone → 5-Bromo-2,3-dimethyl-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Ethyl Ketone | HCID 6569 | — |
| Reactant | 4-Bromophenylhydrazine hydrochloride | HCID 12157 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Bromo-2,3-dimethyl-1H-indole | HCID 12793097 | 67% |
Reaction Steps
Following a published procedure (Gundersen, E. G. U.S. Patent App. Publ. US 2005/070592) 2-Butanone (0.11 mL, 1.278 mmol) was added to a solution of 4-bromophenylhydrazine hydrochloride (0.300 g, 1.342 mmol in EtOH (3.8 mL). The mixture was heated to reflux for 22 h, concentrated in vacuo, and partitioned between EtOAc and 1N HCl. The organic layer was washed with H2O and saturated aqueous NaHCO3, dried over Na2SO4, filtered, and concentrated. The crude residue was purified by chromatography (SiO2, 0-20% EtOAc/Hexane) to afford the desired indole as a pink powder (200 mg, 67%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08748473B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-a77b45717ef348488aa1730458407939 |
| Source note | uspto-grants-2014_06 |