HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1034433Generated: October 30, 2026
N,N,N',N'-Tetramethylethylenediamine → (5-Methyl-1-benzofuran-2-yl)boronic acid
https://huagongshe.com/reaction/1034433
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| 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 Steps
n-Butyl lithium (1.7M, 35.16 ml) was added dropwise to a stirred solution of TMEDA (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 warming. 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 | US05317023 |
|---|
| Source dataset | uspto-grants-1994_05 |
|---|
| ORD ID | ord-9c7beb916dcd426199346144dd3081f8 |
|---|
| Source note | uspto-grants-1994_05 |
|---|