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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 127748생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/127748

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물Diethyl EtherHCID 3283—
반응물AcetyleneHCID 6326—
반응물Ammonium ChlorideHCID 25517—
반응물PotassiumHCID 5462222—
반응물2,2-DimethoxypropanalHCID 7568181—
촉매Ferric nitrateHCID 25251—
생성물4,4-Dimethoxy-3-methyl-but-1-yn-3-olHCID 12875227—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04256878
출처 데이터셋uspto-grants-1981_03
ORD IDord-78228a57e3094a31a6b2cbf110a538ac
출처 메모uspto-grants-1981_03