HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1041942Generated: October 27, 2026
Hydrochloric Acid → (4-(1-Hydroxycyclopropyl)phenyl)boronic acid
https://huagongshe.com/reaction/1041942
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate | HCID 2773500 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Catalyst | Titanium isopropoxide | HCID 11026 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (4-(1-Hydroxycyclopropyl)phenyl)boronic acid | HCID 57416393 | — |
Reaction Steps
A 3.0 M solution of ethylmagnesium bromide in diethylether (7.6 mL) is added to a stirred solution of titanium(IV) isopropoxide (2.2 mL) in diethylether (70 mL) chilled to −78° C. The resultant solution is stirred at −78° C. for 1.5 h, before 4-(4,4,5,5-tetramethyl-[1,3,2]dioxa borolan-2-yl)-benzoic acid methyl ester (2.0 g) is added. The reaction mixture is warmed to ambient temperature and stirred for an additional 12 h. Then, 1 M aqueous hydrochloric acid is added and the resulting mixture is extracted with ethyl acetate. The combined organic extracts are dried (sodium sulphate) and the solvent is evaporated. The residue is dissolved in acetone (60 mL) and 0.1 M aqueous NH4OAc solution (50 mL) followed by NaIO4 (2.3 g) is added. The resulting reaction mixture is stirred at room temperature for 18 h. After removal of the acetone, the residue is extracted with ethyl acetate. The combined extracts are dried (sodium sulphate) and the solvent is evaporated. The residue is purified by chromatography on silicagel (cyclohexane/ethyl acetate).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08557782B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-e4d709af50194d6f9bb84e7211db1e33 |
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| Source note | uspto-grants-2013_10 |
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