HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755508Generated: October 27, 2026
Hydrochloric Acid → Dibenzofuran-4-boronic acid
https://huagongshe.com/reaction/1755508
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | 4-Bromodibenzo[b,d]furan | HCID 458256 | — |
| Reactant | HCID 178418244 | HCID 178418244 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Dibenzofuran-4-boronic acid | HCID 2734328 | 80% |
Reaction Steps
In a 300 ml three-necked flask, 7.2 g of 4-bromodibenzofuran was dissolved in −78° C. anhydrous tetrahydrofuran (THF) under an argon atmosphere. Then, 20 ml of an n-butyl lithium-n-hexane solution (1.6 M, 1.1 eq) was added and stirred for 1 hour. 4.23 ml (1.3 eq) of trimethoxyborane (B(OMe)3) was added and stirred for 2 hours, and the temperature of the reaction system was increased to room temperature. 200 ml of 1 N hydrochloric acid was added into the reactant and stirred for 3 hours. An organic layer was separated, and solvents were distilled off. In the crude product thus obtained, hexane was added. Precipitated product was filtered to obtain 4.94 g of dibenzofuran-4-boronic acid as a white solid (yield 80%). The product was measured by FAB-MS, and dibenzofuran-4-boronic acid having a molecular weight of 212 was detected.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09172047B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-eef586b16e714a5088e62021c813b531 |
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| Source note | uspto-grants-2015_10 |
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