関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | Diethyl Ether | HCID 3283 | — |
| 反応物 | Acetylene | HCID 6326 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | Potassium | HCID 5462222 | — |
| 反応物 | 2,2-Dimethoxypropanal | HCID 7568181 | — |
| 触媒 | Ferric nitrate | HCID 25251 | — |
| 生成物 | 4,4-Dimethoxy-3-methyl-but-1-yn-3-ol | HCID 12875227 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04256878 |
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| 出典データセット | uspto-grants-1981_03 |
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| ORD ID | ord-78228a57e3094a31a6b2cbf110a538ac |
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| 出典メモ | uspto-grants-1981_03 |
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