HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 241995Erstellt: 23. Oktober 2026
Triethylamine → Ethyl 2-diazo-3-(2-fluorophenyl)-3-oxopropanoate
https://huagongshe.com/de/reaction/241995
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Ethyl 3-(2-fluorophenyl)-3-oxopropanoate | HCID 296342 | — |
| Edukt | 4-Acetamidobenzenesulfonyl azide | HCID 5129185 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | Ethyl 2-diazo-3-(2-fluorophenyl)-3-oxopropanoate | HCID 76818128 | — |
Reaktionsschritte
Ethyl 3-(2-fluorophenyl)-3-oxopropanoate (1.00 g, 4.76 mmol) was dissolved in acetonitrile (14 mL) and treated with triethylamine (0.760 ml, 5.47 mmol, 1.15 equiv). The mixture was cooled to 0° C., treated with 4-acetamidobenzenesulfonylazide (1.26 g, 5.23 mmol, 1.1 equiv) and warmed to ambient temperature over 1.5 hours. The mixture was partially concentrated in vacuo, cooled to 0° C., treated with sodium hydroxide (50 mL, 1 N aqueous) and extracted with chloroform (3×50 mL). The combined organic extracts were dried with sodium sulfate, filtered and concentrated in vacuo. The residue was purified via silica gel gradient chromatography (100:0 to 85:15; hexanes:ethyl acetate) providing the titled compound as a yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08653079B2 |
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| Quelldatensatz | uspto-grants-2014_02 |
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| ORD ID | ord-6ab024c191ed49abb57df564e3e0ab5e |
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| Quellennotiz | uspto-grants-2014_02 |
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