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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 36561Erstellt: 23. Oktober 2026

Acetone Cyanohydrin → 2-(4-Methylsulphonyl-2-nitrobenzoyl)-5,5-dimethylcyclohexane-1,3-dione

https://huagongshe.com/de/reaction/36561

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetone CyanohydrinHCID 6406—
EduktTriethylamineHCID 8471—
EduktDimedoneHCID 31358—
Edukt4-(Methanesulfonyl)-2-nitrobenzoyl chlorideHCID 14800186—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-(4-Methylsulphonyl-2-nitrobenzoyl)-5,5-dimethylcyclohexane-1,3-dioneHCID 1993713948,8%

Reaktionsschritte

A solution of 4-methylsulphonyl-2-nitrobenzoyl chloride (9.62 g) in dry dichloromethane (50 ml) was added to a stirred solution of triethylamine (5.6 ml) and 5,5-dimethylcyclohexane-1,3-dione (5 g) in dry dichloromethane (70 ml) during 30 minutes and the reaction mixture stirred at ambient temperature for 4 hours. Triethylamine (15.3 ml) and acetone cyanohydrin (0.5 ml) were added successively and the reaction mixture stirred at ambient temperature for 18 hours. The reaction mixture was washed successively with 2N hydrochloric acid (2×50 ml) and water (2×50 ml), dried over magnesium sulphate and evaporated under reduced pressure to give a yellow glass which was recrystallised from methanol (20 ml) to give 2-(4-methylsulphonyl-2-nitrobenzoyl)-5,5-dimethylcyclohexane-1,3-dione (6.4 g), m.p. 156.5°-158° C., as a yellow crystalline solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05416061
Quelldatensatzuspto-grants-1995_05
ORD IDord-d58fcbdd740644d9af498b7e9b6eb406
Quellennotizuspto-grants-1995_05