HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-bromo-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Ethyl 1-(benzenesulfonyl)indole-2-carboxylate | HCID 506886 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-bromo-1H-indole | HCID 11805631 | — |
Reaction Steps
To a stirred solution of ethyl 1-phenylsulfonylindole-2-carboxylate (1 eq.) in DMF (2.5 ml/mmol) under N2, was added a solution of bromine (4 eq.) in DMF (0.5 ml/mmol). This reaction mixture was stirred at room temperature for about 4 hours, following which water was added and the mixture was extracted with dichloromethane (×3). The organic layer was washed with a saturated solution of Na2SO5, dried and evaporated to give a crude yellow oil. Purification by chromatography on silica gel (eluent: C6H12/EtOAc 9/1) afforded 3-brominated indole 11.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07534809B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-d55ecee6241546d6bf04101ce3512fd9 |
| Source note | uspto-grants-2009_05 |