HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 456791Erstellt: 24. Oktober 2026
Hydrochloric Acid → 4,4-Diethoxy-1-(4-nitrophenyl)but-2-yn-1-one
https://huagongshe.com/de/reaction/456791
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 3,3-Diethoxypropyne | HCID 66285 | — |
| Edukt | N-methoxy-N-methyl-4-nitrobenzamide | HCID 2991007 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 4,4-Diethoxy-1-(4-nitrophenyl)but-2-yn-1-one | HCID 18438594 | — |
Reaktionsschritte
3,3-Diethoxyprop-1-yne (8.5 ml, 59 mmol) was dissolved in THF (100 ml). The solution was cooled to −70° C., and nBuLi (19 ml of 2.5 M soln in hexanes, 47.5 mmol) was added over 5 min. The solution was warmed to 0° C. for 15 min, then cooled to −70 ° C. again. A solution of N-methoxy-N-methyl-4-nitrobenzamide (Intermediate 8, 8.04 g, 38.1 mmol) in THF (50 ml) was added dropwise over 15 min. The solution was warmed to 0° C. after 15 min, and held there for 45 min. The reaction mixture was poured into 1M HCl, extracted with ethyl acetate and dried over sodium sulfate. Purification by chromatography on silica gel eluting with 30 to 50% dichloromethane: hexane, gave the title compound as a light orange oil which solidified on standing (7.14 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07186738B2 |
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| Quelldatensatz | uspto-grants-2007_03 |
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| ORD ID | ord-52ad3e59f4f24aa3a7736f9b578531f6 |
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| Quellennotiz | uspto-grants-2007_03 |
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