HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455899Generated: October 30, 2026
Hydrochloric Acid → 3-Benzyloxy-phenylboronic acid
https://huagongshe.com/reaction/1455899
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | Boronic Acid | HCID 61668 | — |
| Reactant | 1-(Benzyloxy)-3-bromobenzene | HCID 2756638 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Benzyloxy-phenylboronic acid | HCID 2734313 | — |
Reaction Steps
The 3-benzyloxybromobenzene of formula IV is converted to the boronic acid derivative by dissolving in THF and adding one equivalent of n-butyllithium at -78° C. After stirring at -78° C. for approximately 30 minutes, one equivalent of triisopropyl borate is added and the reaction is slowly warmed to room temperature, followed by acidification with aqueous hydrochloric acid to give a 3-benzyloxybenzene boronic acid compound of formula V. ##STR7##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05843940 |
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| Source dataset | uspto-grants-1998_12 |
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| ORD ID | ord-471dccf2c1fa46e28376187520642c3c |
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| Source note | uspto-grants-1998_12 |
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