HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 397120Erstellt: 24. Oktober 2026
tert-Butanol → Methyl 2-((tert-butoxycarbonyl)amino)-3-nitrobenzoate
https://huagongshe.com/de/reaction/397120
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | tert-Butanol | HCID 6386 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Edukt | 2-(Methoxycarbonyl)-6-nitrobenzoic acid | HCID 4399477 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Methyl 2-((tert-butoxycarbonyl)amino)-3-nitrobenzoate | HCID 9965968 | 70% |
Reaktionsschritte
To a solution of methyl 2-carboxy-3-nitrobenzoate (7.23 g) in DMF (50 ml) was added diphenylphosphoryl azide (11.3 g) at room temperature and then triethylamine (6.7 ml) was added dropwise to the stirred reaction mixture. After stirring at room temperature for 3 hours, tert-butanol (54 ml) was added to the stirred reaction mixture. After stirring at room temperature for 30 min., the reaction mixture was gradually warmed, then heated under reflux for 1 hour and evaporated to dryness. The resultant residue was dissolved in ethyl acetate, washed with dilute hydrochloric acid, aqueous sodium bicarbonate, and water, and then dried. After evaporation of the solvent, methanol was added to the resultant residue and the mixture was cooled to give colorless crystals (6.7 g, 70%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06608210B2 |
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| Quelldatensatz | uspto-grants-2003_08 |
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| ORD ID | ord-ee547fd9936a4114ac0b1c5cb01b93e1 |
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| Quellennotiz | uspto-grants-2003_08 |
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