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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284229Generated: October 25, 2026

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

https://huagongshe.com/reaction/1284229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantAcetic AnhydrideHCID 7918—
ReactantHydrogen iodideHCID 24841—
Reactant5-(3-Ethoxypropyl)-5-hydroxy-dibenzo[a,d]cyclohepteneHCID 23328862—
Product5-(3-iodopropyl)-5H-dibenzo[a,d]cyclohepteneHCID 23328868—

Reaction Conditions

Temperature65 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03978121
Source datasetuspto-grants-1976_08
ORD IDord-c513c1fe2498427f8684e5bd10a21bab
Source noteuspto-grants-1976_08