HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1436375Erstellt: 25. Oktober 2026
tert-Butanol → Ethyl 1-((tert-butoxycarbonyl)amino)cyclopropanecarboxylate
https://huagongshe.com/reaction/1436375
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | tert-Butanol | HCID 6386 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Edukt | 1-(Ethoxycarbonyl)cyclopropanecarboxylic acid | HCID 11789472 | — |
| Produkt | Ethyl 1-((tert-butoxycarbonyl)amino)cyclopropanecarboxylate | HCID 10242916 | 91% |
Reaktionsschritte
Triethylamine (29.82 mL, 214 mmol) was added under nitrogen dropwise to a mixture of 1,1-cyclopropanedicarboxylic acid monoethyl ester (31.518 g, 199 mmol), prepared in the previous step, and diphenylphosphoryl azide (47.4 mL, 219 mmol) in 40 mL of tert-butanol at room temperature. After the addition, the reaction was refluxed for 5 h. The reaction was concentrated under reduced pressure. The residue was taken up in ethyl acetate and extracted three times each with 5% citric acid, saturated NaHCO3 and saturated NaCl. The ethyl acetate layer was dried (anhydrous MgSO4), filtered and the solvent removed under reduced pressure to give 1-[[(1,1-dimethylethoxy)carbonyl]amino]cyclopropane carboxylic acid ethyl ester (41.3931 g, 91%) as a yellow oil, MS (ES) m/z 130.0 [M+H-tBoc].
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07618990B2 |
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| Quelldatensatz | uspto-grants-2009_11 |
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| ORD ID | ord-2ed34a90c5f0453b9150e0fa309f4594 |
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| Quellennotiz | uspto-grants-2009_11 |
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