HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triisopropyl borate → (6-Methoxy-1-benzothiophen-2-yl)boronic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | 6-Methoxy-1-benzothiophene | HCID 13634237 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (6-Methoxy-1-benzothiophen-2-yl)boronic acid | HCID 10560276 | 71% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a solution of 6-methoxybenzo[b]thiophene (Graham, S. L., et al. J. Med. Chem. 1989, 32, 2548-2554)(18.13 g, 0.111 mol) in 150 mL of anhydrous THF at -60° C. was added n-BuLi (76.2 mL, 0.122 mol, 1.6 M solution in hexanes), dropwise via syringe. After stirring for 30 min, triisopropyl borate (28.2 mL, 0.122 mol) was introduced via syringe. The resulting mixture was allowed to gradually warm to 0° C. and then partitioned between 1.0 N HCl and EtOAc (300 mL each). The layers were separated, and the organic phase was dried over Na2SO4. Concentration in vacuo produced a white solid that was triturated from Et2O/hexanes. Filtration provided 16.4 g (71%) of 6-methoxybenzo[b]thiophene-2-boronic acid as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06025382 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-17136e36bfcc45079fd2cbde0bc8509a |
| Source note | uspto-grants-2000_02 |