Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Hexanethiol | HCID 8106 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,3-Dichloropyrazine | HCID 78575 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22413525 | HCID 22413525 | — |
Reaction Steps
Hexanethiol (4.7 g, 40 mmole) was added to a slurry of sodium hydride (0.96 g) in THF (60 ml), and the mixture stirred for 30 minutes. The slurry was cooled to -5° C. and a solution of 2,3-dichloropyrazine (6 g) added. The mixture was stirred for 1.5 hours, filtered and the filtrate evaporated. The residue was purified by column chromatography on silica gel using varying concentrations of methanol in chloroform. Fractions containing the desired product were evaporated, yielding 2-chloro-3-hexylsulfanyl pyrazine. as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05512574 |
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| Source dataset | uspto-grants-1996_04 |
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| ORD ID | ord-1043458148a145cf9edb4c31b7bb4af8 |
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| Source note | uspto-grants-1996_04 |
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