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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 414647Erstellt: 25. Oktober 2026

Hydrochloric Acid → 1-Chloro-4-carbomethoxy cyclohexane

https://huagongshe.com/reaction/414647

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktMethyl AcrylateHCID 7294—
EduktChloropreneHCID 31369—
EduktAluminum(III) ChlorideHCID 6451240—
EduktMethyl 4-chlorocyclohex-3-ene-1-carboxylateHCID 14365658—
Edukt1-Chloro-5-carbomethoxy cyclohexeneHCID 14365659—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-Chloro-4-carbomethoxy cyclohexaneHCID 21281591—

Reaktionsbedingungen

Temperatur22 °C

Reaktionsschritte

A mixture of 200 parts of anhydrous aluminum chloride in 2000 parts of methylene chloride was maintained under an atmosphere of nitroge while 129 parts of methyl acrylate was added over a period of about 0.5 hours. With the addition of the methyl acrylate, the temperature of the mixture rose exothermically to about 34° C. The mixture was cooled to about 22° C. and 132.8 parts of freshly prepared chloroprene was added slowly, with stirring over a period of about 1.5 hours. During the addition, the temperature rose slowly to reflux condition (about 40° C.). The reaction mixture was then maintained under a nitrogen atmosphere, with stirring, for about 16 hours at ambient conditions. The crude reaction product was then treated with 10% HCl, and washed with methylene chloride and distilled to yield an essentially pure mixture of 1-chloro-4-carbomethoxy cyclohexene (92%) and its isomer 1-chloro-5-carbomethoxy cyclohexene (8%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04792618
Quelldatensatzuspto-grants-1988_12
ORD IDord-0a3b4868c83541a398d89ec083c5ebff
Quellennotizuspto-grants-1988_12