HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 487022Erstellt: 24. Oktober 2026
Diphenylacetylene → 1,1-Dimethyl 2,3-diphenyl-2-cyclopropene-1,1-dicarboxylate
https://huagongshe.com/de/reaction/487022
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diphenylacetylene | HCID 10390 | — |
| Edukt | 2-Diazonio-1,3-dimethoxy-3-oxoprop-1-en-1-olate | HCID 547673 | — |
| Katalysator | Bis(pentane-2,4-dione-kappa~2~O~2~,O~4~)copper | HCID 45052134 | — |
| Produkt | 1,1-Dimethyl 2,3-diphenyl-2-cyclopropene-1,1-dicarboxylate | HCID 12809034 | 26,8% |
Reaktionsschritte
A 100 millilater round-bottom flask was equipped with a magnetic stirrer and reflux condenser with N2 inlet. The flask was charged with 25.0 grams (0.140 mole) of diphenylacetylene and 140 milligrams of cupric acetylacetonate. The mixture was heated to 120° C. using an oil bath and 8.85 grams (0.056 mole) of dimethyl diazomalonate was added over 24 hours using a syringe pump. When all of the dimethyl diazomalonate had been added, heating at 120° C. was continued for 8 hours. The diphenylacetylene was distilled off under vacuum, boiling point 170° C./19 Mm. The residue was purified by flash chromatography eluting with 75:25 hexane-ethyl acetate to give 4.65 grams (0.015 mole) of the desired product as a white solid. NMR analysis of the product indicated the following:
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05292937 |
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| Quelldatensatz | uspto-grants-1994_03 |
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| ORD ID | ord-66d65d320ac04264a52aa06affbf25cc |
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| Quellennotiz | uspto-grants-1994_03 |
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