HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 623693Erstellt: 24. Oktober 2026
4-Fluorophenylhydrazine hydrochloride → 2-(4-fluorophenyl)-4-methyl-2H-1,2,3-triazole 1-oxide
https://huagongshe.com/de/reaction/623693
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Fluorophenylhydrazine hydrochloride | HCID 69981 | — |
| Edukt | Isonitrosoacetone | HCID 6399095 | — |
| Katalysator | Copper sulfate pentahydrate | HCID 24463 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | 2-(4-fluorophenyl)-4-methyl-2H-1,2,3-triazole 1-oxide | HCID 90111509 | 94,9% |
Reaktionsschritte
To a stirred solution of anti-pyruvic aldehyde 1-oxime (3.4 g, 39 mmol) in diethyl ether (75 mL) was added 4-fluorophenylhydrazine hydrochloride (5.85 g, 36 mmol). The reaction mixture was stirred at 23° C. for 16 h, and then concentrated under reduced pressure. The crude residue was dissolved in pyridine (120 mL). A solution of copper(II) sulfate pentahydrate (18 g, 72 mmol) in water (55 mL) was added dropwise over 4 min. The resulting mixture was stirred at reflux for 2 h. The mixture was concentrated under reduced pressure to remove excess pyridine. To the mixture was added 1.0 M aqueous hydrochloric acid. The mixture was extracted with ethyl acetate and the organic layer was separated and washed with 1.0 M aqueous hydrochloric acid until a clear amber organic layer was obtained. The organic layer was dried (MgSO4), filtered, and evaporated under reduced pressure to afford the title compound (6.6 g) as a colorless solid. The title compound was used directly in the next step without further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09302999B2 |
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| Quelldatensatz | uspto-grants-2016_04 |
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| ORD ID | ord-80c695a5e9c641f3a17b8e5a9a48124c |
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| Quellennotiz | uspto-grants-2016_04 |
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