HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1774Erstellt: 23. Oktober 2026
2-Aminobenzophenone → 2-(5-Oxotetrahydrofuran-2-carbonyl)aminobenzophenone
https://huagongshe.com/de/reaction/1774
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2-Aminobenzophenone | HCID 76080 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 2-(5-Oxotetrahydrofuran-2-carbonyl)aminobenzophenone | HCID 53932370 | — |
Reaktionsschritte
A mixture of 4.9 g of 5-oxotetrahydrofuran-2-carboxylic acid and 5.5 ml of thionyl chloride was subjected to reflux for 2 hours. Thionyl chloride was then distilled off under reduced pressure to leave 5-oxotetrahydrofuran-2-carbonyl chloride. This product was mixed with 5.0 g of 2-aminobenzophenone, 200 ml of ethyl acetate and 200 ml of a saturated aqueous solution of sodium hydrogencarbonate, which was stirred for one hour at room temperature. The ethyl acetate layer was washed with water and dried over anhydrous magnesium sulfate, then the solvent was distilled off under reduced pressure. The residue was purified by means of a silica gel column chromatography (eluent, hexane:ethyl acetate=2:1) to give 2-(5-oxotetrahydrofuran-2-carbonyl)aminobenzophenone (6.5 g) as needles, m.p. 100° C.-102° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05726306 |
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| Quelldatensatz | uspto-grants-1998_03 |
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| ORD ID | ord-947d3e4afae94a0b8dd4f97535b58d90 |
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| Quellennotiz | uspto-grants-1998_03 |
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