HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triisopropyl borate → (5-Methyl-1-benzofuran-2-yl)boronic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | 5-Methylbenzofuran | HCID 33103 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (5-Methyl-1-benzofuran-2-yl)boronic acid | HCID 15680843 | — |
Reaction Conditions
| Temperature | -10 °C |
|---|
Reaction Steps
n-Butyl lithium (35.16 ml) was added dropwise to a stirred solution of THEDA (9.58 ml) and 5-methylbenzofuran (8.22 g) in ether (250 ml) maintaining the temperature below -60° C. throughout. The solution was warmed to about -10° C. over 45 minutes and stirred at this temperature for 30 minutes. A precipitate formed on warning. The suspension was cooled and triisopropylborate (43 ml) was added, maintaining the temperature below -60° C. The solution was warmed gradually to room temperature before quenching with 2N HCl (70 ml). The mixture was extracted with ether (3×50 ml) and the combined organic extracts washed with 2N HCl (4×30 ml), water (2×30 ml) and dried before evaporation to give the title compound as an orange solid (12.75 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05310927 |
| Source dataset | uspto-grants-1994_05 |
| ORD ID | ord-b26d0fcca28a42ee84273a20909565ea |
| Source note | uspto-grants-1994_05 |