HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 378523Erstellt: 24. Oktober 2026
tert-Butanol → 6-(((Tert-butoxy)carbonyl)amino)pyridine-2-carboxylic acid
https://huagongshe.com/de/reaction/378523
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | tert-Butanol | HCID 6386 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 2,6-Pyridinedicarboxylic acid | HCID 10367 | — |
| Edukt | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Produkt | 6-(((Tert-butoxy)carbonyl)amino)pyridine-2-carboxylic acid | HCID 22726931 | — |
Reaktionsschritte
To a suspension of 2,6-pyridinedicarboxylic acid (8.35 g, 50 mmol) and triethylamine (5.05 g, 50 mmol) in tert-butyl alcohol (ca. 60 mL) was dropwise added diphenylphosphoryl azide (13.8 g, 50 mmol), and the mixture was stirred at room temperature until the reaction mixture became a clear solution. The solution was then slowly heated and refluxed for 2.5 hour. After cooling, the mixture was partitioned between ethyl acetate/hexane (1:1, v/v) and 1% aqueous sodium hydroxide. The organic layer was washed again with 1% aqueous sodium hydroxide. All the aqueous solutions were combined and neutralized to pH=5 with concentrated hydrochloric acid in the presence of ethyl acetate. The ethyl acetate layer was washed with brine, dried over sodium sulfate and concentrated to obtain 5.0 g of 6-tert-butoxycarbonylamino-2-pyridinecarboxylic acid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06030965 |
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| Quelldatensatz | uspto-grants-2000_02 |
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| ORD ID | ord-90433118cead4a0b91bd2ff96b3947a0 |
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| Quellennotiz | uspto-grants-2000_02 |
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