Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzene | HCID 241 | — |
| Edukt | Acetylene | HCID 6326 | — |
| Edukt | Dimethylcyanamide | HCID 15112 | — |
| Katalysator | Cobaltocene | HCID 92884 | — |
| Produkt | 2-Dimethylaminopyridine | HCID 21885 | — |
Reaktionsschritte
3.1 gm. of cobaltocene (0.016 mole) under nitrogen was dissolved in 44.0 gm. of benzol. The solution mixed with 164 gm. of anhydrous N,N-dimethylcyanamide (2.3 moles). The reaction mixture was saturated with 12 atm. of acetylene at 20° C. in a 1-liter autoclave (with stirring). The reaction mixture was heated to 70° C. Then at the beginning of the exothermal reaction, the heating was carefully increased so that a temperature of 160° C. prevailed in the autoclave. After a drop in pressure in the autoclave to below 12 atm., acetylene was repressed on. After 10 hours of reaction time, the autoclave was cooled down and expansion allowed. As a result of fractional distillation, 238 gm. of 2-(N,N-dimethylamino)-pyridine (boiling point: 92° C., 21 torr) was obtained, after benzol and a small quantity of N,N-dimethylcyanamide had been obtained. The 2-(N,N-dimethylamino)-pyridine had a purity of 99.8 percent--this corresponded to a yield of 84.5 percent.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04196287 |
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| Quelldatensatz | uspto-grants-1980_04 |
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| ORD ID | ord-5d85a4687cd74782a6762d5c68f1f304 |
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| Quellennotiz | uspto-grants-1980_04 |
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