HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 352136Erstellt: 24. Oktober 2026
Diethyl Ether → [4-(2-Methoxy-pyridin-3-yl)-4-oxo-butyl]-carbamic acid tert-butyl ester
https://huagongshe.com/de/reaction/352136
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | Diisopropylamine | HCID 7912 | — |
| Edukt | 2-Methoxypyridine | HCID 74201 | — |
| Edukt | [2-(Methoxymethyl-carbamoyl)-ethyl]-carbamic acid tert-butyl ester | HCID 86584230 | — |
| Edukt | HCID 178418348 | HCID 178418348 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | [4-(2-Methoxy-pyridin-3-yl)-4-oxo-butyl]-carbamic acid tert-butyl ester | HCID 102539314 | — |
Reaktionsschritte
2-Methoxypyridine (1.9 ml) and then diisopropylamine (0.1 ml) were added to a solution of methyl lithium (10 ml of a 1.6M solution in ether) in tetrahydrofuran (20 ml) at −78° C. and the solution was stirred at 0° C. for 18hand then re-cooled to −78° C. A solution of 1,1-dimethylethyl [3-(methoxymethylamino)-3-oxopropyl]-carbamate (1.6 g) in tetrahydrofuran (5 ml) was added slowly and the resultant solution was allowed to warm to −30° C. over 3.5 h, quenched with aqueous ammonium chloride and extracted with ether (three times). The combined organic extracts were dried (sodium sulphate), evaporated and purified by chromatography on silica eluting with petrol-ether gave the sub-title compound as a colourless oil (0.572 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06743939B2 |
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| Quelldatensatz | uspto-grants-2004_06 |
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| ORD ID | ord-3e38315d28f442a38cbf626afe239183 |
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| Quellennotiz | uspto-grants-2004_06 |
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