HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 550030Erstellt: 26. Oktober 2026
Hydrochloric Acid → 3-(Difluoromethoxy)benzeneboronic acid
https://huagongshe.com/reaction/550030
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Triisopropyl borate | HCID 21531 | — |
| Edukt | (Difluoromethoxy)benzene | HCID 68015 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 3-(Difluoromethoxy)benzeneboronic acid | HCID 17750069 | 57,6% |
Reaktionsschritte
A solution of 3-(difluoromethoxy)benzene (3.0 g) and triisopropoxyborane (2.78 g) in tetrahydrofuran (15 ml) was cooled to −78° C. under argon atmosphere, and thereto was added a solution of n-butyl lithium (1.59 M hexane solution, 9.3 ml). The mixture was stirred at same temperature for 10 minutes, warmed, and further stirred at room temperature overnight. Thereto was added 3N aqueous hydrochloric acid solution (10 ml), and the mixture was stirred at room temperature for 5 minutes. The mixture was extracted with ethyl acetate. The extract was washed with brine, and dried over sodium sulfate. The solvent was evaporated under reduced pressure. The residue was crystallized from hexane to give 3-difluoromethoxybenzene-boronic acid (1.6 g) as colorless crystals.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07943788B2 |
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| Quelldatensatz | uspto-grants-2011_05 |
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| ORD ID | ord-ca943c1872314cb7a36f550cfacaeb53 |
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| Quellennotiz | uspto-grants-2011_05 |
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