HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethyl borate → (6-Isopropyldibenzo[b,d]furan-4-yl)boronic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 4-Isopropyldibenzo[b,d]furan | HCID 15691990 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (6-Isopropyldibenzo[b,d]furan-4-yl)boronic acid | HCID 86684644 | 77% |
Reaction Steps
n-Butyl lithium (81 mL, 130 mmol) was added slowly to 4-isopropyldibenzo[b,d]furan (10.9 g, 51.8 mmol) in 100 mL dry THF at −78° C. This mixture was allowed to stir at room temperature for 5 hours and then cooled back to −78° C. Trimethyl borate (20.23 mL, 181 mmol) was added slowly to the reaction and the reaction allowed to warm up to room temperature overnight. The reaction was poured into 100 mL NH4OH solution with ice. The mixture was extracted with 3×100 mL ethyl acetate, dried over sodium sulfate, evaporated and crystallized from DCM/hexane to yield 10.1 g (77%) of the desired product, which was confirmed by NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09193745B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-1de2f35b0328450f8742329981e85153 |
| Source note | uspto-grants-2015_11 |