HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 380128Erstellt: 24. Oktober 2026
2-Bromo-1,2-diphenylethan-1-one → 2-Oxo-1,2-diphenylethyl 1-(3-benzyloxybenzoyl)-2-piperidinecarboxylate
https://huagongshe.com/de/reaction/380128
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2-Bromo-1,2-diphenylethan-1-one | HCID 102630 | — |
| Edukt | Sodium | HCID 5360545 | — |
| Edukt | 1-(3-Benzyloxybenzoyl)-2-piperidinecarboxylic acid | HCID 18367416 | — |
| Katalysator | Sulfuric Acid | HCID 1118 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 2-Oxo-1,2-diphenylethyl 1-(3-benzyloxybenzoyl)-2-piperidinecarboxylate | HCID 54247856 | 28,4% |
Reaktionsschritte
Sodium (54 mg) was dissolved in ethanol (8.0 ml), and then 1-(3-benzyloxybenzoyl)-2-piperidinecarboxylic acid (665 mg), conc. sulfuric acid (1 drop), and desyl bromide (539 mg) was successively dissolved thereto. The resulting mixture was stirred at 70° C. for 2 days, cooled to room temperature, and partitioned between ethyl acetate and 1N HCl. The organic layer was washed with 1N HCl, aqueous sodium bicarbonate, and brine, dried over MgSO4, and evaporated in vacuo. The residue was chromatographed over silica gel to afford 2-oxo-1,2-diphenylethyl 1-(3-benzyloxybenzoyl)-2-piperidinecarboxylate (297 mg) as a pale yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06300344B1 |
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| Quelldatensatz | uspto-grants-2001_10 |
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| ORD ID | ord-969536c747cd4b3a94fb701bec284060 |
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| Quellennotiz | uspto-grants-2001_10 |
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