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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706773Generated: October 30, 2026

3,5-Dichloropyrazine-2-carbaldehyde → 3,5-Dichloro-α-methyl-2-pyrazinemethanol

https://huagongshe.com/reaction/706773

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Dichloropyrazine-2-carbaldehydeHCID 15696840—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
Product3,5-Dichloro-α-methyl-2-pyrazinemethanolHCID 15696846—

Reaction Steps

3,5-Dichloro-pyrazine-2-carbaldehyde (5.0 g) was dissolved in dry tetrahydrofuran (100 ml) in a reaction vessel equipped with a magnetic stirring bar under an argon atmosphere. The solution was cooled on an ice-bath before slow addition of 10.3 ml methylmagnesium bromide solution (3M in tetrahydrofuran), keeping the internal temperature in the reaction vessel below 5° C. After the addition the cooling bath was removed and the reaction mixture stirred for another 10 min. Then the reaction mixture was quenched with a saturated aqueous sodium bicarbonate solution (100 ml) and extracted with EtOAc (3×200 ml). The combined aqueous phases were dried over sodium sulfate, filtered and evaporated to afford 1-(3,5-dichloro-pyrazin-2-yl)-ethanol as a dark brown oil. Yield: 5.23 g (96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174993B2
Source datasetuspto-grants-2015_11
ORD IDord-cdb559d2fcd44d82b66170f0e8120ebe
Source noteuspto-grants-2015_11