HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850316Generated: October 26, 2026
Hydrochloric Acid → 2,5-Dichlorobenzeneboronic acid
https://huagongshe.com/reaction/850316
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | 1,4-Dichloro-2-iodobenzene | HCID 122452 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2,5-Dichlorobenzeneboronic acid | HCID 2773371 | — |
Reaction Steps
To a cold (-78° C.) solution of 2,5-dichloroiodobenzene (50 g) and triisopropoxyborane (46.5 ml) in tetrahydrofuran (500 ml) was added dropwise n-butyllithium in hexane (1.69 M, 119 ml). The mixture was stirred at -78° C. for 30 minutes. The reaction mixture was poured into 2M hydrochloric acid solution (180 ml) and stirred for 10 minutes. The product was extracted with ether (200 ml) 2 times, and the organic layers were combined, washed with brine, dried over magnesium sulfate and evaporated in vacuo. To the residue was added n-hexane (60 ml) and the crystalline was collected, washed with n-hexane and dried to give 2,5-dichlorophenyl-dihydroxyborane (21.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06017917 |
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| Source dataset | uspto-grants-2000_01 |
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| ORD ID | ord-bd440742ec8a42bcb1426dd4542885a8 |
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| Source note | uspto-grants-2000_01 |
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