HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → 4-methyl-1H-indol-5-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5-Methoxy-4-methylindole | HCID 3296242 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-methyl-1H-indol-5-ol | HCID 21691244 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
5-Methoxy-4-methyl-1H-indole (10 g, 62.0 mmol) is dissolved in DCM (400 mL) and cooled to 0° C. BBr3 (155 mL, 155 mmol) is added dropwise over 1 hour and the black mixture is allowed to warm to room temperature overnight (17 hours). The reaction is poured over a mixture of ice and sodium bicarbonate (aq) solution and extracted with ethyl acetate (1.5 L) and concentrated to a black oil. The oil is absorbed onto silica and separated via FCC (0-50% ethyl acetate:heptanes) to obtain the title compound as a solid. MS (ESI) m/z 148.23 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08492393B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-67fde889ef054469a85f0a1cffebd7a1 |
| Source note | uspto-grants-2013_07 |