HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → 6-Hydroxyindole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 6-Methoxy-1H-indole | HCID 76659 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Hydroxyindole | HCID 524508 | — |
Reaction Steps
6-Methoxyindole (1.47 g, 10.00 mmol) was cooled to 0° C. in methylene chloride and BBr3 (2 M in methylene chloride, 25 mL, 50.00 mmol) was added. After stirring 16 h at room temperature, TLC analysis indicated the reaction was complete. The reaction was quenched with water and the layers separated. The organic layers were washed with 1 N NaOH. The basic aqueous layers were acidified with conc. HCL, extracted with methylene chloride, dried over anhydrous magnesium sulfate, and concentrated in vacuo to give the crude 6-hydroxyindole which was used directly for the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06777437B2 |
| Source dataset | uspto-grants-2004_08 |
| ORD ID | ord-99b017107f31491986d9e36245860446 |
| Source note | uspto-grants-2004_08 |