HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 5-Ethoxymethoxy-2-methylphenylboronic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 2-Bromo-4-ethoxymethoxy-1-methylbenzene | HCID 22345586 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Ethoxymethoxy-2-methylphenylboronic acid | HCID 22345604 | 87% |
Reaction Steps
1.4 g (59 mmol) of magnesium turnings are placed in tetrahydrofuran in a round-bottomed flask and under a stream of nitrogen. 13.2 g (54 mmol) of 2-bromo-4-ethoxymethoxy-1-methylbenzene diluted in a small amount of THF are added slowly. The medium is refluxed for 20 minutes. It is then added via a cannula to 15 ml (65 mmol) of triisopropyl borate. The mixture sets to a solid and is then poured into 1N hydrochloric acid solution and extracted with ether. The organic phase is dried over magnesium sulfate, filtered and then evaporated. 9.8 g (87%) of the expected product are obtained in the form of a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06924400B2 |
| Source dataset | uspto-grants-2005_08 |
| ORD ID | ord-229c39ba6be9404ebf6c654717af294a |
| Source note | uspto-grants-2005_08 |