HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1480911Erstellt: 26. Oktober 2026
3-Methylbut-1-yne → 1-(5-chloro-2-nitro-phenyl)-5-isopropyl-1H-[1,2,3]triazole
https://huagongshe.com/reaction/1480911
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 3-Methylbut-1-yne | HCID 69019 | — |
| Edukt | 2-Azido-4-chloro-1-nitrobenzene | HCID 11229390 | — |
| Edukt | HCID 178418918 | HCID 178418918 | — |
| Edukt | HCID 178446074 | HCID 178446074 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1-(5-chloro-2-nitro-phenyl)-5-isopropyl-1H-[1,2,3]triazole | HCID 59428156 | — |
Reaktionsschritte
A 30 mL scintillation vial was charged with 2-azido-4-chloro-1-nitrobenzene (200 mg, 1.0 mmol) and 0.75 M 3-methyl-1-butynylmagnesium chloride in THF (1.6 mL, 1.2 mmol; prepared by mixing 3-methyl-1-butyne (120 L, 1.2 mmol) and iPrMgCl (1.5 mL, 1.0 M in THF) at room temperature, heating to 40° C. for 30 minutes then cooling to room temperature). The reaction was allowed to stir at room temperature for 1 hour after which the reaction was quenched with SiO2 and the solvent removed. The product (adsorbed to SiO2) was then loaded on a SiO2 column and purified to give 1-(5-chloro-2-nitro-phenyl)-5-isopropyl-1H-[1,2,3]triazole.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09409909B2 |
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| Quelldatensatz | uspto-grants-2016_08 |
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| ORD ID | ord-96942e336d9e4fd6bb5d8781f3c39f84 |
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| Quellennotiz | uspto-grants-2016_08 |
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