HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → (3,5-Di-tert-butylphenyl)boronic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | 1-Bromo-3,5-di-tert-butylbenzene | HCID 620136 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3,5-Di-tert-butylphenyl)boronic acid | HCID 11470330 | — |
Reaction Steps
3,5-Di-t-butylbromobenzene (10 g, 37 mmol) and magnesium (1.8 g, 75 mmol) were dissolved in 100 mL of THF and stirred at reflux for five hours. After this time, triisopropylborate (7.0 g, 37 mmol) as a solution in diethylether (50 mL) was added to the solution, followed by stirring at room temperature overnight. Then the THF was removed in vacuo to leave a crude oil. This oil was taken up in 100 mL of diethylether and 100 mL of 10% sulfuric acid (aqueous) and stirred for two hours. The organic layer was separated and neutralized with saturated sodium bicarbonate solution, whereafter the solvent was removed in vacuo to yield a white solid. The solid is washed generously with pentane. Yield: 3.0 g (34%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07157591B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-d3cb5e0c0bd0482e8fbf66b041214858 |
| Source note | uspto-grants-2007_01 |