HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 68221Erstellt: 24. Oktober 2026
Potassium Carbonate → tert-Butyl 3-oxocyclobutylcarbamate
https://huagongshe.com/de/reaction/68221
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | tert-butyl N-(3-methylidenecyclobutyl)carbamate | HCID 28875369 | — |
| Katalysator | Tetrabutylammonium Chloride | HCID 70681 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | tert-Butyl 3-oxocyclobutylcarbamate | HCID 23374584 | 177,6% |
Reaktionsschritte
To a vigorously stirring solution of N-Boc-3-methylene-cyclobutanamine (9.8 g, 53.5 mmol) in DCM (160 mL) and H2O (160 mL) was added K2CO3 (3 g, 21.7 mmol), followed by NaClO4 (35 g, 163.5 mmol), tetrabutylammonium chloride (0.2 g, 0.72 mmol) and RuCl3 (0.6 g, 7.6 mmol). During the course of the reaction, the organic solution turned dark brown, the catalyst turned black, while the upper aqueous layer turned white. The reaction was monitored by TLC, and upon completion, the reaction mixture was filtered through a pad of celite. The filtrates were transferred to a separatory funnel, and the aqueous layer was extracted with DCM (2×50 mL). The combined organic layers were washed with 5% NaHCO3 (2×30 mL), brine (30 mL), dried over Na2SO4, filtered and evaporated to dryness to yield a crude, which was purified by flash chromatography (silica gel/hexanes:ethyl acetate 0-60%) to yield the desired N-Boc-3-amino-cyclobutanone (7.13 g, 38.53 mmol, 72% yield): NMR (250 MHz, CDCl3) δ 4.88 (bs, 1H), 4.13-4.29 (m, 1H), 3.23-3.41 (m, 2H), 2.9-3.05 (m, 2H), 1.39 (s, 9H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08822424B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-44c9661632504064abfdcf13d1a6d774 |
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| Quellennotiz | uspto-grants-2014_09 |
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