HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 341689Erstellt: 25. Oktober 2026
Hydrochloric Acid → 3,5-Dimethylbiphenyl-4-ylboronic acid
https://huagongshe.com/reaction/341689
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Trimethyl borate | HCID 8470 | — |
| Edukt | 3,5-Dimethylbiphenyl | HCID 86927 | — |
| Edukt | HCID 178418306 | HCID 178418306 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2-Methylpentane | HCID 7892 | — |
| Produkt | 3,5-Dimethylbiphenyl-4-ylboronic acid | HCID 59450481 | 186,1% |
Reaktionsschritte
tert-Butyllithium (1.7 M solution in hexane, 36.2 ml, 61.6 mmol) is added dropwise to a solution of 3,5-dimethylbiphenyl (7.27 g, 28 mmol) in dry tetrahydrofuran (150 ml) at −78° C. under an atmosphere of nitrogen. The reaction mixture is stirred at −78° C. for 30 minutes, then trimethylborate (9.54 ml, 84 mmol) is added. The resulting mixture is stirred at −78° C. for 30 minutes and then allowed to warm to room temperature. The reaction mixture is acidified with 10% aqueous hydrochloric acid solution and extracted with diethyl ether (2×150 ml). The organic layers are combined, dried over anhydrous magnesium sulfate, filtered and the filtrate is evaporated under reduced pressure to give a yellow solid. Trituration with isohexane gives 3,5-dimethylbiphen-4-ylboronic acid as a white powder (5.89 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08895761B2 |
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| Quelldatensatz | uspto-grants-2014_11 |
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| ORD ID | ord-9b668601273d45edbebdb6c48cea7c55 |
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| Quellennotiz | uspto-grants-2014_11 |
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