HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 460658Erstellt: 25. Oktober 2026
Dimethylformamide → alpha-(2'-(2,3-Epoxypropan-1-yloxy)benzylidene)-gamma-butyrolactone
https://huagongshe.com/reaction/460658
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 3-(2-Hydroxybenzylidene)dihydrofuran-2(3h)-one | HCID 229758 | — |
| Edukt | Oxiran-2-ylmethyl 4-nitrobenzenesulfonate | HCID 286832 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | alpha-(2'-(2,3-Epoxypropan-1-yloxy)benzylidene)-gamma-butyrolactone | HCID 72642278 | 99,1% |
Reaktionsschritte
Dimethylformamide (30 ml) and potassium carbonate (4.4 g) were added to α-(2′-hydroxybenzylidene)-γ-butyrolactone (3 g), and a racemic compound of glycidyl nosylate (3.4 g) was added. The mixture was stirred at 50° C. for 3 hr. Water was added and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to give oily α-(2′-(2,3-epoxypropan-1-yloxy)benzylidene)-γ-butyrolactone (3.2 g). This compound (0.4 g) was reacted in methanol with 4-(naphthalen-2-yl)piperidine (0.5 g) in the same manner as in Example 307 to give the title compound, melting point 127–128° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07196199B2 |
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| Quelldatensatz | uspto-grants-2007_03 |
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| ORD ID | ord-b4fe74838dec4c33a54134100278b4aa |
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| Quellennotiz | uspto-grants-2007_03 |
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