Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | 4-Bromopyridine | HCID 14268 | — |
| Edukt | n-Butyl lithium | HCID 61028 | — |
| Edukt | Diethylmethoxyborane | HCID 522516 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Sodium chloride; water | HCID 57417360 | — |
| Produkt | 4-(Diethylboranyl)pyridine | HCID 13318871 | — |
Reaktionsschritte
N-Butyllithium (1.6M in hexanes, 20 ml) was added to dry ether (100 ml) and cooled to −40° C. under nitrogen. The solution was stirred and a solution of 4-Bromopyridine (32 mmols) dissolved in dry ether was added drop wise. The ethereal solution was stirred for 30 minutes at −40° C. then cooled to −70° C. Diethyl methoxy borane (4.6 ml) dissolved in dry ether (50 ml) was added drop wise and the mixture was allowed to warm to room temperature over night. Ethyl acetate (100 ml) and brine (70 ml) were added to the resulting brown solution and the organic layer was separated. This was dried over magnesium sulfate, filtered and evaporated to yield a brown tar. The product was purified by column chromatography on silica eluted with toluene to yield (0.94 g, 6.4 mmols) of Diethyl (4-pyridyl borane) (I) as a white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08647827B2 |
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| Quelldatensatz | uspto-grants-2014_02 |
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| ORD ID | ord-5f209412a0e34e0d8cf7cf77a42a0b89 |
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| Quellennotiz | uspto-grants-2014_02 |
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