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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1613014Erstellt: 25. Oktober 2026

Hydrochloric Acid → 1-(4-Dimethylaminophenyl)-4,4-dimethylpentane-1,3-dione

https://huagongshe.com/reaction/1613014

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktPinacoloneHCID 6416—
EduktSodium hydrideHCID 24758—
EduktEthyl 4-(dimethylamino)benzoateHCID 25127—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-(4-Dimethylaminophenyl)-4,4-dimethylpentane-1,3-dioneHCID 1895448270%

Reaktionsschritte

Into a 100 ml three-necked flask equipped with a stirrer, a dropping funnel, a reflux condenser, and a nitogen-inlet tube, were charged 2.08 gm (31 mmol) of 60% sodium hydride and 5.0 gm (26 mmol) of ethyl 4-dimethylaminobenzoate. The mixture was dispersed in 40 ml of tetrahydrofuran and heated under refluxing. To the mixture was dropwise added 3.0 gm (30 mmol) of pinacolone and the mixture was heated with stirring for 3 hours. After cooling, 50 ml of 1N hydrochloric acid was added to the reaction mixture, and the organic layer was extracted twice with chloroform. The extract was thoroughly washed with water and dried over anhydrous magnesium sulfate. The solvent was removed by evaporation to obtain an yellow oil. The oily substance was submitted to the Kugelrohr distillation 150° C., 1 mmHg, and crystallized from hexane to give 4.5 gm (yield: 70%) of yellow solid product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05191121
Quelldatensatzuspto-grants-1993_03
ORD IDord-a9e0d73991a74236b05a0ce7ac58645c
Quellennotizuspto-grants-1993_03