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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 225367Erstellt: 23. Oktober 2026

Acetylene → 1-Chloro-trans-1-octen-3-one

https://huagongshe.com/de/reaction/225367

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetyleneHCID 6326—
EduktHexanoyl chlorideHCID 67340—
EduktAluminum(III) ChlorideHCID 6451240—
LösungsmittelCarbon TetrachlorideHCID 5943—
Produkt1-Chloro-trans-1-octen-3-oneHCID 11041003—

Reaktionsschritte

To a slurry of 233.5 g. (1.75 moles) of aluminum chloride in 390 ml. of carbon tetrachloride, saturated with acetylene and cooled in an ice bath, is added over 20 minutes 201.9 g. (150 moles) of hexanoyl chloride. After the addition is complete, acetylene is bubbled into the mixture is rapidly as it is absorbed and for 1 hour after absorption becomes slow. The mixture is poured onto 1700 g. of ice and 720 ml. of saturated brine. The organic phase is separated and the aqueous phase is washed with ether. The combined organic phase and washings are washed with saturated brine, dried (Na2SO4) and evaporated. The residual oil is combined with 10 g. of hydroquinone and distilled to yield a colorless oil, b.p. 51°-52° C. (0.10 torr.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04236027
Quelldatensatzuspto-grants-1980_11
ORD IDord-fb7c836d1a0f4c95beebfdf7357e46fb
Quellennotizuspto-grants-1980_11