HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10099Generated: October 25, 2026
Potassium Iodide → 2,2,2-trifluoro-1-(7-iodo-4,5-dihydro-1H-1,5-methanobenzo[d]azepin-3(2H)-yl)ethanone
https://huagongshe.com/reaction/10099
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 3-(trifluoroacetyl)-2,3,4,5-tetrahydro-1H-1,5-methano3-benzazepin-7-amine | HCID 21864716 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 2,2,2-trifluoro-1-(7-iodo-4,5-dihydro-1H-1,5-methanobenzo[d]azepin-3(2H)-yl)ethanone | HCID 21864725 | — |
Reaction Steps
1-(4-Amino-10-aza-tricyclo[6.3.1.02,7]dodeca-2(7),3,5-trien-10-yl)-2,2,2-trifluoro-ethanone (500 mg, 1.85 mmol) was dissolved in H2O (5 mL) and concentrated H2SO4 solution (0.5 mL) then cooled to 0° C. and treated with a solution of sodium nitrite (NaNO2) (140 mg, 2.04 mmol) in H2O (2 mL) dropwise. Potassium iodide (460 mg, 2.78 mmol) in 1N H2SO4 solution (0.5 mL) was added over 10 minutes (reaction becomes dark red). The resulting solution was warmed to room temperature and stirred 18 hours. The reaction was quenched with NaHSO3 and water (pH 2.5) then extracted with ethyl acetate (4×30 mL). After drying (Na2SO4), the solution was filtered and concentrated to a yellow oil which was chromatographed on Silica gel to provide a yellow oil. (260 mg, 37%). (TLC 30% ethyl acetate/hexanes Rf 0.70). (A 5.4 g scale performed as above yielded 5 g, 67%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07091372B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-61f22df1abf941a0bb796b93e209b430 |
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| Source note | uspto-grants-2006_08 |
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