HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553906Generated: October 30, 2026
Iodine → (6R*,9aS*)-6-(3-fluorophenyl)-3-iodooctahydroquinolizin-4-one
https://huagongshe.com/reaction/553906
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | (6R*,9aS*)-6-(3-fluorophenyl)octahydroquinolizin-4-one | HCID 69071146 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (6R*,9aS*)-6-(3-fluorophenyl)-3-iodooctahydroquinolizin-4-one | HCID 69075941 | 103.3% |
Reaction Steps
Iodotrimethylsilane (0.34 mL) was added to a solution of (6R*,9aS*)-6-(3-fluorophenyl) octahydroquinolizin-4-one (383 mg) and N,N,N′,N′-tetramethylethylenediamine (0.82 mL) in methylene chloride (15 mL) under ice-cooling in a nitrogen atmosphere, and the reaction solution was stirred under ice-cooling for 30 minutes. Iodine (590 mg) was added to the reaction solution under ice-cooling, and the reaction solution was stirred under ice-cooling for one hour. Ethyl acetate and a saturated sodium thiosulfate solution were added to the reaction solution, and the organic layer was separated. The resulting organic layer was washed with brine, dried over magnesium sulfate, and then concentrated under reduced pressure to obtain 597 mg of the title compound. The property value of the compound is as follows.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08048878B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-ad84cbae4c9a420282e4f6bafe4bb616 |
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| Source note | uspto-grants-2011_11 |
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