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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 597556Erstellt: 25. Oktober 2026

Benzaldehyde → 1,3-Diphenyl-2-methyl-1,3-propandione

https://huagongshe.com/reaction/597556

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehydeHCID 240—
EduktDimethylformamideHCID 6228—
EduktSodium CyanideHCID 8929—
Edukt3-(Dimethylamino)-1-phenyl-1-propanoneHCID 77042—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
Produkt1,3-Diphenyl-2-methyl-1,3-propandioneHCID 344637—

Reaktionsschritte

A solution of 21.2 g (0.2 mol) of benzaldehyde and 100 ml of absolute dimethylformamide is added dropwise in the course of 1/2 hour to a mixture of 9.8 g (0.2 mol) of NaCN and 100 ml of absolute dimethylformamide in a manner analogous to Example 3. Stirring is continued for 21/2 hours at 35° C. A solution of 26.6 g (0.15 mol) of dimethyl-β-benzoyl-ethylamine and 100 ml of absolute dimethylformamide is then slowly added dropwise in the course of 2 hours. Stirring is continued for 2 hours at the same temperature and water is then added to the reaction mixture in three times its quantity. The reaction product precipitates immediately. After cooling in an ice bath, the precipitated product is suction filtered and thoroughly washed with water. 34.3 g of crude product are isolated. 21.6 g (60.5% of the theory) of dibenzoyl ethane are isolated by recrystallisation from ethanol; m.p. 143° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04014889
Quelldatensatzuspto-grants-1977_03
ORD IDord-1edd11de3330483aa6ca975150942e01
Quellennotizuspto-grants-1977_03