HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477744Generated: October 30, 2026
Cyanogen Bromide → HCID 19872310, compound
https://huagongshe.com/reaction/477744
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | HCID 772049 | HCID 772049 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19872310 | HCID 19872310 | 66.4% |
Reaction Steps
3-Benzylthio-1-phenyl-1,2,4-triazole (5 g) in dry tetrahydrofuran (50 ml) at -70° C. was treated dropwise with n-butyllithium (1.05 equivs). The solution was stirred at -70° C. for 10 minutes and cyanogen bromide (1.98 g) was added rapidly. The mixture was allowed to warm to room temperature and was then quenched with ethanol. The volatile materials were removed in vacuo, and the crude product was chromatographed on silica using dichloromethane to give 4.3 g of the desired product as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04889553 |
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| Source dataset | uspto-grants-1989_12 |
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| ORD ID | ord-15bb7797a8c0414aa1ebc044f8bcd0b9 |
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| Source note | uspto-grants-1989_12 |
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