HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45567Generated: October 29, 2026
Diethyl Ether → 2-Phenyl-3-methoxypyrazine
https://huagongshe.com/reaction/45567
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Butyl ether | HCID 8909 | — |
| Reactant | 2-Methoxypyrazine | HCID 18467 | — |
| Reactant | HCID 178506676 | HCID 178506676 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Phenyl-3-methoxypyrazine | HCID 14920499 | 12% |
Reaction Steps
First, in a three-neck flask, 11.30 g of 2-methoxypyrazine and 200 mL of diethylether were put, and a dibutyl ether solution (2.1 mol/L) of phenyl lithium was dropped thereto while the mixture was cooled down with ices and stirred under a nitrogen atmosphere, and stirred to be reacted for 20 hours. After the reaction, water was added to the reaction solution, and an organic layer was extracted with ethyl acetate. The obtained organic layer was washed with water, and dried with magnesium sulfate. Magnesium sulfate was removed by filtration and the solvent was distilled off. The obtained residue was refined with a column chromatography using dichloromethane as a development solvent, so that 2-phenyl-3-methoxypyrazine was obtained (light yellow powder, yield: 12%). A synthesis scheme of Step 1 is shown by the following (a2-1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08541574B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-66c0084a01944f83a4f46360efaa19c3 |
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| Source note | uspto-grants-2013_09 |
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