Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | 2-Methylpyrazine | HCID 7976 | — |
| Edukt | Butyl ether | HCID 8909 | — |
| Edukt | HCID 178506676 | HCID 178506676 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 2-Methyl-3-phenylpyrazine | HCID 12568828 | 22% |
Reaktionsschritte
First, in a nitrogen atmosphere, 50 mL of a dibutyl ether solution containing phenyl lithium (produced by Wako Pure Chemical Industries, Ltd, 2.1 mol/L) and 250 mL of diethylether were mixed. Then, 8.98 g of 2-methylpyrazine (produced by Tokyo Chemical Industries Co., Ltd) was dropped into this solution while the solution was being cooled with ice, and stirred at a room temperature for three hours. Water was added into the reacted solution and an organic layer was extracted with diethylether. The obtained organic layer was washed with water and dried with magnesium sulfate. After the solvent was distilled off, the obtained residue was purified by column chromatography using dichloromethane as a developing solvent, thereby obtaining a pyrazine derivative Hmppr (yellow oily matter, yield: 22%). A synthesis scheme of Step 1 is shown by the following (a-1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09187689B2 |
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| Quelldatensatz | uspto-grants-2015_11 |
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| ORD ID | ord-2bd2ed02403a4baab64126dacee7c0f8 |
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| Quellennotiz | uspto-grants-2015_11 |
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