HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 25015Erstellt: 23. Oktober 2026
Hydrochloric Acid → Ethyl 4-(4-(2,6-difluorobenzyloxy)phenyl)-3-oxobutyrate
https://huagongshe.com/de/reaction/25015
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Pyridine | HCID 1049 | — |
| Edukt | 2,2-Dimethyl-1,3-dioxane-4,6-dione | HCID 16249 | — |
| Edukt | 4-(2,6-Difluorobenzyloxy)benzylcarbonyl chloride | HCID 21964509 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Ethyl 4-(4-(2,6-difluorobenzyloxy)phenyl)-3-oxobutyrate | HCID 21964507 | — |
Reaktionsschritte
To a solution of Meldrum's acid (0.846 g, 5.8 mmol) in dichloromethane (5 ml) was added pyridine (2 ml) over a period of 10 minutes at 0° C. To this solution was added 4-(2,6-Difluorobenzyloxy)benzylcarbonyl chloride (Step D, 1.71 g, 5.7 mmol) in dichloromethane (5 ml), which resulted in an orange solution. The dark orange solution was stirred for 1 hour at 0° C., allowed to warm to room temperature and stirred for an additional hour. The reaction mixture was diluted with dichloromethane and poured onto 2M HCl and ice. The phases were separated and the aqueous phase was extracted twice with dichloromethane. The combined organic layers were washed twice with 2M HCl and brine, dried over Na2SO4, filtered and concentrated to a solid. The solid was suspended in abs EtOH (15 ml) and refluxed for 2.5 hours. The solvent was removed in vacuo to give a dark oil. The residue was purified by flash chromatography on silica gel column (hex:ethyl acetate, 2:1) to provide the title compound as a white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06858602B2 |
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| Quelldatensatz | uspto-grants-2005_02 |
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| ORD ID | ord-0e41a935a22a43f7b0ecc02577376e47 |
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| Quellennotiz | uspto-grants-2005_02 |
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