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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 542639Erstellt: 24. Oktober 2026

Methyl vinyl ketone → 9-Carbamoyl-9-(3-oxobutyl)fluorene

https://huagongshe.com/de/reaction/542639

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl vinyl ketoneHCID 6570—
EduktBenzyltrimethylammonium hydroxideHCID 66854—
Edukt9H-fluorene-9-carboxamideHCID 345028—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt9-Carbamoyl-9-(3-oxobutyl)fluoreneHCID 13853488—

Reaktionsbedingungen

Temperatur45 °C

Reaktionsschritte

To a stirred warm (45° C.) solution of 62.7 g. (0.3 mole) of 9-carbamoylfluorene in 700 ml. of tetrahydrofuran were added in one portion 30 ml. of a 40% aqueous solution of benzyltrimethylammonium hydroxide. The reaction mixture was stirred at 45° C. for fifteen minutes, and was then diluted by dropwise addition of 24.5 g. (0.35 mole) of methyl vinyl ketone. The reaction mixture was heated at reflux for three hours following complete addition, and then it was cooled to about 30° C. and added to 500 g. of ice. The aqueous reaction mixture was extracted several times with 50% diethyl ether in ethyl acetate, and the extracts were combined, washed with water, with 10% aqueous sodium hydroxide, again with water and then dried. Removal of the solvent by evaporation under reduced pressure afforded a solid which, following crystallization from ethyl acetate, was identified as 46.1 g. of 9-carbamoyl-9-(3-oxobutyl)fluorene. m.p. 125°-128° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04658061
Quelldatensatzuspto-grants-1987_04
ORD IDord-78b2e50548b7400f8b7e73a040a3fcf4
Quellennotizuspto-grants-1987_04