Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127748Generated: October 25, 2026

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

https://huagongshe.com/reaction/127748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantDiethyl EtherHCID 3283—
ReactantAcetyleneHCID 6326—
ReactantAmmonium ChlorideHCID 25517—
ReactantPotassiumHCID 5462222—
Reactant2,2-DimethoxypropanalHCID 7568181—
CatalystFerric nitrateHCID 25251—
Product4,4-Dimethoxy-3-methyl-but-1-yn-3-olHCID 12875227—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04256878
Source datasetuspto-grants-1981_03
ORD IDord-78228a57e3094a31a6b2cbf110a538ac
Source noteuspto-grants-1981_03