HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392337Generated: October 27, 2026
Water → 3,6-Difluoropyrazine-2-carbonitrile
https://huagongshe.com/reaction/392337
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | 6-Fluoro-3-(phenylsulfonyl)-2-pyrazinecarbonitrile | HCID 22662842 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 3,6-Difluoropyrazine-2-carbonitrile | HCID 22662829 | 28% |
Reaction Steps
In 4 mL of dimethyl sulfoxide was dissolved 0.40 g of 6-fluoro-3-(phenylsulfonyl)-2-pyrazinecarbonitrile. After adding 0.44 g of potassium fluoride and 0.10 g of tetra-n-butylammonium bromide successively, the mixture thus obtained was stirred at 60° C. for 1.5 hours. The reaction mixture was poured into a mixture of 20 mL of ethyl acetate and 20 mL of water, and the organic layer was separated. The organic layer was washed successively with water and saturated aqueous solution of sodium chloride and dried on anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue was purified by silica gel column chromatography [eluent: n-hexane:ethyl acetate=20:1] to obtain 0.06 g of 3,6-difluoro-2-pyrazinecarbonitrile as a colorless solid product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06800629B2 |
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| Source dataset | uspto-grants-2004_10 |
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| ORD ID | ord-a9313c13ab9d46d886a9c2fbeb3efc27 |
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| Source note | uspto-grants-2004_10 |
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