HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 500075Erstellt: 25. Oktober 2026
1-Diethoxyphosphorylpropan-2-one → HCID 178467819, Verbindung
https://huagongshe.com/reaction/500075
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Diethoxyphosphorylpropan-2-one | HCID 14028 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | HCID 178453955 | HCID 178453955 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | HCID 178467819 | HCID 178467819 | 81,3% |
Reaktionsschritte
To a suspension of 60% sodium hydride (366 mg) and anhydrous tetrahydrofuran (50 ml) under ice-cooling was added diethyl 2-oxopropylphosphonate (1.78 g). The mixture was stirred for 15 minutes and then a solution of t-butyl trans-4-formylcyclohexylcarbamate (1.38 g) in anhydrous tetrahydrofuran (10 ml) was added thereto under the same condition. The mixture was stirred at room temperature for 3 hours, and then saturated aqueous ammonium chloride was added to the reaction mixture. The mixture was extracted with toluene, and the organic layer was washed with brine, dried over sodium sulfate, and then the solvent was removed in vacuo. The residue was purified by a silica gel chromatography (eluent: gradient from 100% hexane/0% ethyl acetate to 0% hexane/100% ethyl acetate) to give 1.32 g of t-butyl trans-4-[(E)-3-oxo-1-butenyl]cyclohexylcarbamate.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07767854B2 |
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| Quelldatensatz | uspto-grants-2010_08 |
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| ORD ID | ord-09453b8b2300498f81cdaea25b684644 |
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| Quellennotiz | uspto-grants-2010_08 |
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