Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ammonia | HCID 222 | — |
| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | Acetylene | HCID 6326 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | Potassium | HCID 5462222 | — |
| Edukt | 2,2-Dimethoxypropanal | HCID 7568181 | — |
| Katalysator | Ferric nitrate | HCID 25251 | — |
| Produkt | 4,4-Dimethoxy-3-methyl-but-1-yn-3-ol | HCID 12875227 | — |
Reaktionsschritte
After the addition of a slight amount of iron (III) nitrate, 2700 ml. of liquid ammonia are treated portion-wise with stirring and cooling with 169.5 g. of potassium. As soon as the initially blue coloration has disappeared, i.e., after about 30-45 minutes, acetylene gas in a stream of 3 l/min. is led in until the dark coloration of the reaction mixture becomes lighter. Then, the gas stream is reduced to 2 l/min. and the mixture treated dropwise with a solution of 500 g. of methylglyoxal-dimethylacetal in 425 ml. of abs. diethyl ether. The introduction of acetylene is continued for 1 hour with stirring. The reaction mixture is subsequently treated portion-wise with 425 g. of ammonium chloride, gradually warmed to 30° C. within 12 hours with evaporation of the ammonia and extracted with 1600 ml. of diethyl ether. The ether extract is dried over sodium sulfate and evaporated under reduced pressure. The remaining 4,4-dimethoxy-3-methyl-but-1-yn-3-ol boils, after rectification, at 33° C./0.03 mm Hg; nD25 =1.4480.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04256878 |
|---|
| Quelldatensatz | uspto-grants-1981_03 |
|---|
| ORD ID | ord-78228a57e3094a31a6b2cbf110a538ac |
|---|
| Quellennotiz | uspto-grants-1981_03 |
|---|