Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395307Generated: October 26, 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/395307

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 numberUS06605610B1
Source datasetuspto-grants-2003_08
ORD IDord-92550d0f471e425fa28f79e0a8c30d33
Source noteuspto-grants-2003_08