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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 127748Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/127748

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
EduktDiethyl EtherHCID 3283—
EduktAcetyleneHCID 6326—
EduktAmmonium ChlorideHCID 25517—
EduktPotassiumHCID 5462222—
Edukt2,2-DimethoxypropanalHCID 7568181—
KatalysatorFerric nitrateHCID 25251—
Produkt4,4-Dimethoxy-3-methyl-but-1-yn-3-olHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04256878
Quelldatensatzuspto-grants-1981_03
ORD IDord-78228a57e3094a31a6b2cbf110a538ac
Quellennotizuspto-grants-1981_03