HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284467Generated: October 31, 2026
Hydrochloric Acid → 4-Cyclopropylbenzeneboronic acid
https://huagongshe.com/reaction/2284467
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | 1-Bromo-4-cyclopropylbenzene | HCID 12221355 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 4-Cyclopropylbenzeneboronic acid | HCID 2849428 | — |
Reaction Steps
2.5 M solution of nButyllithium in hexane (14.5 mL) is added dropwise to 1-bromo-4-cyclopropyl-benzene (5.92 g) dissolved in THF (14 mL) and toluene (50 mL) and chilled to −70° C. The resultant solution is stirred at −70° C. for 30 min before triisopropyl borate (8.5 mL) is added. The solution is warmed to −20° C. and then treated with 4 M aqueous hydrochloric acid (15.5 mL). The reaction mixture is further warmed to room temperature and then the organic phase is separated. The aqueous phase is extracted with ethyl acetate and the combined organic phases are dried (sodium sulfate). The solvent is evaporated and the residue is washed with a mixture of ether and cyclohexane to give the product as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09145434B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-8569aed9cb53473fac9aaf663837f8a4 |
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| Source note | uspto-grants-2015_09 |
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