HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1725183Erstellt: 26. Oktober 2026
Phenacyl bromide → 4-Oxo-4-phenyl-2-(4-propyl-cyclohexanecarbonyl)-butyric acid ethyl ester
https://huagongshe.com/reaction/1725183
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Phenacyl bromide | HCID 6259 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 3-Oxo-3-(4-propyl-cyclohexyl)-propionic acid ethyl ester | HCID 57423720 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Sodium chloride; water | HCID 57417360 | — |
| Produkt | 4-Oxo-4-phenyl-2-(4-propyl-cyclohexanecarbonyl)-butyric acid ethyl ester | HCID 69061689 | 115,5% |
Reaktionsschritte
To a stirred slurry of 0.92 g (23 mmol) NaH, 60% dispersion in mineral oil, in 30 mL anhydrous THF, cooled 0° C. in ice, 5.12 g (21.3 mmol) 3-oxo-3-(4-propyl-cyclohexyl)-propionic acid ethyl ester from Step 2 was added dropwise over the course of 60 min. The reaction was stirred at 0° C. for 1 hr. 2-bromoacetophenone (5.57 g, 28 mmol) in 12 mL anhydrous THF was then added dropwise at 0° C. and the reaction was allowed to stir at room temperature over 5 days. The reaction was poured into brine, extracted with ethyl acetate, dried over MgSO4, and concentrated to afford 8.85 g (24.6 mmol, 115% yield) 4-oxo-4-phenyl-2-(4-propyl-cyclohexanecarbonyl)-butyric acid ethyl ester as an oil. The product was used in the next step without further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07488832B2 |
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| Quelldatensatz | uspto-grants-2009_02 |
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| ORD ID | ord-94058aeecafe4b6dbe3f7ec07bb88595 |
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| Quellennotiz | uspto-grants-2009_02 |
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