HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893108Generated: October 26, 2026
Hydrochloric Acid → 2,3-Diphenylbenzo[b]furan-6-boronic acid
https://huagongshe.com/reaction/1893108
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | 6-Bromo-2,3-diphenylbenzofuran | HCID 59866501 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2,3-Diphenylbenzo[b]furan-6-boronic acid | HCID 59866510 | 60% |
Reaction Steps
Under an argon atmosphere, 400 mL of anhydrous THF were added to 40.2 g of 6-bromo-2,3-diphenylbenzo[b]furan, and the mixture was stirred at −40° C. During the stirring, 72 mL of a 1.6-M solution of n-butyllithium in hexane were added to the mixture. The reaction solution was stirred for 1 hour while being heated to 0° C. The reaction solution was cooled to −78° C. again, and a solution of 54.0 g (250 mmol) of trimethyl borate in 50 mL of dry THF was dropped to the solution. The reaction solution was stirred at room temperature for 5 hours. 200 mL of 1N hydrochloric acid were added to the reaction solution, and the mixture was stirred for 1 hour. After that, the water layer was removed. The organic layer was dried with magnesium sulfate, and the solvent was removed by distillation under reduced pressure. The resultant solid was washed with toluene, whereby 21.7 g of 2,3-diphenylbenzo[b]furan-6-boronic acid were obtained (60% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08512875B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-9e838d81e1d74c73a26f061d92b09f21 |
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| Source note | uspto-grants-2013_08 |
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