HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2384006Generated: October 30, 2026
Hydrochloric Acid → 3-Isopropylbenzeneboronic acid
https://huagongshe.com/reaction/2384006
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | 1-Bromo-3-isopropylbenzene | HCID 138499 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Isopropylbenzeneboronic acid | HCID 2773478 | 93.5% |
Reaction Steps
n-BuLi (7.7 mL, 14.0 mmol) was added dropwise to a stirred solution of 1-bromo-3-isopropyl-benzene (2.4 g, 12.1 mmol) in dry THF (40 mL) over 30 min at −70° C. under nitrogen. The reaction mixture was degassed for 15 min, and triisopropylborate (2.63 g, 14.0 mmol) was added at the same temperature. The reaction mixture was gradually warmed to 0° C. during 90 min and stirred for an additional 30 min at 0° C. The reaction mixture was then cooled to −20° C., and an aqueous solution of 2N HCl (20 mL) was added slowly. THF was distilled off and the reaction mixture was extracted with ethyl acetate (2×20 mL). The combined organic layers were dried over Na2SO4, and concentrated in vacuo to obtain the crude product (1.85 g, 93.5%), which was used for the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08263656B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-fd1ff9c0ecbd4f2ea6b64bbf3f5318db |
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| Source note | uspto-grants-2012_09 |
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