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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantAcetylpyrazineHCID 30914—
ReactantHCID 178462451HCID 178462451—
SolventTetrahydrofuranHCID 8028—
Product2-(Pyrazin-2-yl)but-3-yn-2-olHCID 58221410—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470847B2
Source datasetuspto-grants-2013_06
ORD IDord-302e4674f22a495eb0a6f54675d7fbec
Source noteuspto-grants-2013_06