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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Hydrogen iodide | HCID 24841 | — |
| Reactant | 5-(3-Ethoxypropyl)-5-hydroxy-dibenzo[a,d]cycloheptene | HCID 23328862 | — |
| Product | 5-(3-iodopropyl)-5H-dibenzo[a,d]cycloheptene | HCID 23328868 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03978121 |
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| Source dataset | uspto-grants-1976_08 |
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| ORD ID | ord-c513c1fe2498427f8684e5bd10a21bab |
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| Source note | uspto-grants-1976_08 |
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