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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 5565Erstellt: 24. Oktober 2026

Hydrochloric Acid → 2-Butyryl-5-cyclohexylcyclohexane-1,3-dione

https://huagongshe.com/de/reaction/5565

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktDimethyl malonateHCID 7943—
EduktButyryl chlorideHCID 8855—
EduktSodium HydroxideHCID 14798—
Edukt1-Cyclohexylbut-1-en-3-oneHCID 95597—
EduktSodium MethoxideHCID 10942334—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
Produkt2-Butyryl-5-cyclohexylcyclohexane-1,3-dioneHCID 1979657984,1%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

132 g of dimethyl malonate, 180 g of 30% strength sodium methylate, 152 g of 1-cyclohexylbut-1-en-3-one and 106.5 g of butyryl chloride are reacted in 1 liter of toluene, in a manner similar to that described in Example 1. 5 g of 4-N,N-dimethylaminopyridine are added to the reaction mixture thus obtained and the batch is stirred for 4 hours at 100° C. and then cooled to room temperature. It is then extracted twice with a total of 3.5 moles of sodium hydroxide in 1.5 liters of water and the combined alkaline extracts are stirred for 2 hours at 80° C. They are then acidified with about 270 ml of concentrated hydrochloric acid at 50° C., the oil obtained is extracted with methylene chloride and the extracts are washed with water and evaporated in vacuo. 222 g (84%) of 2-butyryl-5-cyclohexylcyclohexane-1,3-dione are obtained as a pale brown oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05245041
Quelldatensatzuspto-grants-1993_09
ORD IDord-c5320739ecb94875895071e346290d87
Quellennotizuspto-grants-1993_09