HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 614383Generated: October 25, 2026
Butyl iodide → 4-Butoxycarbonyl-5-(pyrazin-2-yl)-1,2-dithiole-3-thione
https://huagongshe.com/reaction/614383
Participants
| Role | Name | HCID | Charge |
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| Reactant | Butyl iodide | HCID 10962 | — |
| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 4-Carboxy-5-(pyrazin-2-yl)-1,2-dithiole-3-thione | HCID 21329166 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Butoxycarbonyl-5-(pyrazin-2-yl)-1,2-dithiole-3-thione | HCID 21329175 | 25.6% |
Reaction Steps
Anhydrous hexamethylphosphotriamide (5 cc) and 4-carboxy-5-(pyrazin-2-yl)-1,2-dithiole-3-thione (1.28 g) (prepared as described in Example 32) are added to a solution of dry sodium ethoxide (0.34 g) in anhydrous ethanol (5 cc). The suspension obtained is heated to a temperature of about 50° C., the resulting solution is cooled to a temperature of about 20° C. and then butyl iodide (1.7 g) is added. The reaction mixture is then maintained at a temperature of about 50° C. for 7 hours. An insoluble material is filtered off and the filtrate is evaporated to dryness under reduced pressure (20 mm Hg). The oil obtained is treated with ethyl acetate (2 cc) and the product which crystallises is filtered off and washed with diethyl ether (2 cc). After drying, 4-butoxycarbonyl-5-(pyrazin-2-yl)-1,2-dithiole-3-thione (0.4 g), melting at 127° C., is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04144339 |
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| Source dataset | uspto-grants-1979_03 |
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| ORD ID | ord-fd28bd04fdf44a3396e7397a9d05a45b |
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| Source note | uspto-grants-1979_03 |
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