HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508002Generated: October 30, 2026
3,5-Dichloropyrazine-2-carbaldehyde → 3,5-Dichloro-α-methyl-2-pyrazinemethanol
https://huagongshe.com/reaction/1508002
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3,5-Dichloropyrazine-2-carbaldehyde | HCID 15696840 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3,5-Dichloro-α-methyl-2-pyrazinemethanol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09221828B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-b01ce719d4a74d288c2dcc15f0f24c18 |
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| Source note | uspto-grants-2015_12 |
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