Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 1,4-Dioxane | HCID 31275 | — |
| Edukt | Phenyl Trifluoromethanesulfonate | HCID 548641 | — |
| Edukt | Phenylborate | HCID 19793864 | — |
| Produkt | Phenylboronic acid pinacol ester | HCID 570673 | — |
Reaktionsschritte
In a reaction tube under nitrogen, a mixture of PdCl2(dppf)CH2Cl2 (23 mg; 0.028 mmol) and triethylamine (0.36 ml; 2.58 mmol) in dioxane (4 ml; dried over 4 Å sieves) was sealed and stirred at 80° C. overnight (18 h). After cooling to room temperature, 1.29M HB(pin) in dioxane (1.00 ml; 1.29 mmol) and phenyl trifluoromethanesulfonate (197 mg; 0.871 mmol) were added and the reaction mixture was stirred at 80° C. GC analysis after 4 days showed a new peak at 7.4 minutes which was identified by GC/MS as the desired phenylborate compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07122694B2 |
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| Quelldatensatz | uspto-grants-2006_10 |
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| ORD ID | ord-95b5015a277441deb8b9b0428ff19a15 |
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| Quellennotiz | uspto-grants-2006_10 |
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