HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260585Generated: November 2, 2026
Ethyl Acetate → 2-(Pyrazin-2-yl)but-3-yn-2-ol
https://huagongshe.com/reaction/1260585
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Acetylpyrazine | HCID 30914 | — |
| Reactant | HCID 178462451 | HCID 178462451 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Pyrazin-2-yl)but-3-yn-2-ol | HCID 58221410 | — |
Reaction Steps
A 0.5 M solution of ethynylmagnesium chloride in tetrahydrofuran (31.90 mmol, Aldrich) is diluted with 50 ml of tetrahydrofuran and then cooled to 0° C. 3 g of 1-pyrazin-2-ylethanone (24.56 mmol, Lancaster) are then added in several fractions, and the mixture is stirred at 0° C. for 4 hours. The mixture is cooled once again with an ice bath and a solution of NH4Claq is added slowly. The mixture is extracted twice with ethyl acetate and the organic phases are then combined, dried over sodium sulphate, filtered, and concentrated under vacuum. The oily residue obtained is purified by silica chromatography (elution with a cyclohexane:ethyl acetate gradient, 70:30 to 50:50) and 2.9 g of the expected product are obtained in the form of a yellow oil (yield=80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08470847B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-302e4674f22a495eb0a6f54675d7fbec |
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| Source note | uspto-grants-2013_06 |
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