HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351072Generated: October 25, 2026
Hydrochloric Acid → (2-Phenoxyphenyl)boronic acid
https://huagongshe.com/reaction/1351072
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diphenyl Ether | HCID 7583 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | n-Butyl lithium | HCID 61028 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-Phenoxyphenyl)boronic acid | HCID 2773559 | — |
Reaction Steps
Diphenyl ether (0.85 g) was dissolved in anhydrous tetrahydrofuran (20 ml) and the reaction mixture was cooled to 0° C. N-butyllithium (1.6M, 3.1 ml) was delivered by drops thereto and the reaction mixture was stirred for 30 minutes at the same temperature. Trimethyl borate (0.68 ml) was added thereto and the reaction mixture was stirred for two hours at room temperature. 1N hydrochloric acid was added to the reaction mixture and the water layer was extracted with ethyl acetate. The organic layer was dried with anhydrous sodium sulfate. The solvent was distilled off and the obtained residue was purified by column chromatography (ethyl acetate:hexane=1.5:1 to 1:3) to obtain the title compound (304 mg) having the following physical data.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07217701B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-fc9a122849a04f92b889fb2a05817b76 |
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| Source note | uspto-grants-2007_05 |
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