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HRID 460958作成日:2026年10月27日

Ammonia → 4,4-Dimethoxy-3-methyl-but-1-yn-3-ol

https://huagongshe.com/reaction/460958

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物Diethyl EtherHCID 3283—
反応物AcetyleneHCID 6326—
反応物Ammonium ChlorideHCID 25517—
反応物PotassiumHCID 5462222—
反応物2,2-DimethoxypropanalHCID 7568181—
触媒Ferric nitrateHCID 25251—
生成物4,4-Dimethoxy-3-methyl-but-1-yn-3-olHCID 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 1/min. is led in until the dark coloration of the reaction mixture becomes lighter. Then, the gas stream is reduced to 2 1/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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04061656
出典データセットuspto-grants-1977_12
ORD IDord-215c5c98a62e48fb846b5bddf096acae
出典メモuspto-grants-1977_12