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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-AminobenzophenoneHCID 76080—
EduktSodium BicarbonateHCID 516892—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-(5-Oxotetrahydrofuran-2-carbonyl)aminobenzophenoneHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05726306
Quelldatensatzuspto-grants-1998_03
ORD IDord-947d3e4afae94a0b8dd4f97535b58d90
Quellennotizuspto-grants-1998_03