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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2071717Erstellt: 26. Oktober 2026

Iodine → 5-(3-iodopropyl)-5H-dibenzo[a,d]cycloheptene

https://huagongshe.com/reaction/2071717

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktAcetic AnhydrideHCID 7918—
EduktHydrogen iodideHCID 24841—
Edukt5-(3-Ethoxypropyl)-5-hydroxy-dibenzo[a,d]cyclohepteneHCID 23328862—
Produkt5-(3-iodopropyl)-5H-dibenzo[a,d]cyclohepteneHCID 23328868—

Reaktionsbedingungen

Temperatur65 °C

Reaktionsschritte

A solution of 9.25 g. (0.0314 mole) of 5-(3-ethoxypropyl)-5-hydroxy-dibenzo[a,d]cycloheptene prepared as above in 45 ml. of acetic anhydride is heated on the steam-bath for 90 minutes then cooled to 65° C. A stream of nitrogen is passed through the solution while 30 ml. of hydriodic acid (sp. gr., 1.5) is added in portions, keeping the temperature below 90° C. The solution develops a dark brown iodine color during the addition. The solution is heated to 80° C. for 30 minutes, then cooled and poured into ice-water. The brown oil that separates is extracted into benzene and the extract washed with water, dilute sodium thiosulfate solution and finally with water. Evaporation of the benzene gives the product 5-(3-iodopropyl)-5H-dibenzo-[a,d]cycloheptene as a yellow oil. A sample gives a precipitate with alcoholic silver nitrate solution.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04048223
Quelldatensatzuspto-grants-1977_09
ORD IDord-90149e9f64074e5b8b5067c8ee640539
Quellennotizuspto-grants-1977_09