HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 390809Erstellt: 24. Oktober 2026
N,N,N',N'-Tetramethylethylenediamine → Methyl 3-((tert-butoxycarbonyl)amino)furan-2-carboxylate
https://huagongshe.com/de/reaction/390809
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Edukt | Dimethyl Carbonate | HCID 12021 | — |
| Edukt | tert-butyl N-(furan-3-yl)carbamate | HCID 12207186 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Methyl 3-((tert-butoxycarbonyl)amino)furan-2-carboxylate | HCID 52987670 | 51% |
Reaktionsschritte
To a solution of tert-butyl furan-3-ylcarbamate 32 (1.7 g, 1.0 eq) in THF (50 ml) at −30° C. was added TMEDA (1.75 ml, 1.3 eq) followed by 1.6M solution of n-butyllithium (8.4 ml, 2.25 eq, 1.6M in hexanes). Reaction mixture was allowed to warm up to 0° C. and stirred for 1 h, before being cooled back to −30° C. Dimethyl carbonate (2.4 ml, 3.0 eq) was quickly added, before the reaction mixture was allowed to warm up to room temperature for 1 hr. Reaction mixture was quenched with 2M HCl, followed by addition of saturated aq. NaCl. Mixture was extracted with ethyl acetate. The combined organic extracts were dried with Na2SO4 and concentrated. The crude reaction mixture was purified by flash chromatography to yield tert-butyl 2-(methoxycarbonyl)furan-3-ylcarbamate 33 (1.14 g, 51%): MS (Q1) 242 (M)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08383620B2 |
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| Quelldatensatz | uspto-grants-2013_02 |
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| ORD ID | ord-fb3a4c3755864f2c88bff16ca71e6767 |
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| Quellennotiz | uspto-grants-2013_02 |
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