HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → 2-Methylbenzofuran-6-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 6-Methoxy-2-methylbenzofuran | HCID 13013073 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Methylbenzofuran-6-ol | HCID 12203498 | 54.2% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a stirred solution of 6-Methoxy-2-methyl-benzofuran 125-A (1.76 g, 10.85mmol) in 45 ml of CH2Cl2 at −5° C. was added BBr3 (24 ml of 1M BBr3 in CH2Cl2, 16 28 mmol). The reaction was allowed to warm to 0° C. and stirred at that temperature for 1.5 hr. The reaction was poured into a mixture of ice and saturated aqueous NaHCO3 and layers were separated. The aqueous layer was re-extracted with CH2Cl2. The combined organic layers were dried (MgSO4) and concentrated under reduced pressure to a brown oil. The residue was chromatographed on silica gel eluting CH2Cl2 to give 872 mg (54%) of 6-Hydroxy-2-methyl-benzofuran 125-B.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07381824B2 |
| Source dataset | uspto-grants-2008_06 |
| ORD ID | ord-c56fc70fc36d46b1b8a26688069fc83b |
| Source note | uspto-grants-2008_06 |