HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 450858Generated: October 26, 2026
Benzyltrimethylammonium hydroxide → HCID 178510368, compound
https://huagongshe.com/reaction/450858
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyltrimethylammonium hydroxide | HCID 66854 | — |
| Reactant | 2-Cyanoethanethioamide | HCID 1416277 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 2-Dimethoxymethyl-3-hydroxy-acrylonitrile | HCID 57937103 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 178510368 | HCID 178510368 | — |
Reaction Steps
A suspension of the sodium salt of 2-dimethoxymethyl-3-hydroxy-acrylonitrile (3.94 g, 23.86 mmol) in hydrochloric acid (20 ml, 0.5 M) is heated at 50° C. for 30 minutes. Excess hydrochloric acid is neturalized using triethylamine, before adding cyanoacetothioamide (2.39 g, 23.9 mmol) and a catalytic amound of benzyltrimethylammonium hydroxide. The mixture is stirred at room temperature for two hours, heated at 60° C. for 2 hours and then refluxed for 4 hours. Evaporation of the solvents leaves a solid that is purified on silicagel to yield 3,5-dicyano-2-marcaptopyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08486996B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-0704176d76584d41a772a9f45bc0554a |
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| Source note | uspto-grants-2013_07 |
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