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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457438Generated: October 30, 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/457438

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant3-(trifluoroacetyl)-2,3,4,5-tetrahydro-1H-1,5-methano3-benzazepin-7-amineHCID 21864716—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
Product2,2,2-trifluoro-1-(7-iodo-4,5-dihydro-1H-1,5-methanobenzo[d]azepin-3(2H)-yl)ethanoneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07186870B2
Source datasetuspto-grants-2007_03
ORD IDord-d027a006e336480cb18d1ae852dd0020
Source noteuspto-grants-2007_03