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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzaldehyde | HCID 240 | — |
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Sodium Cyanide | HCID 8929 | — |
| Edukt | 3-(Dimethylamino)-1-phenyl-1-propanone | HCID 77042 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 1,3-Diphenyl-2-methyl-1,3-propandione | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04014889 |
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| Quelldatensatz | uspto-grants-1977_03 |
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| ORD ID | ord-1edd11de3330483aa6ca975150942e01 |
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| Quellennotiz | uspto-grants-1977_03 |
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