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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2218235Generated: November 1, 2026

Potassium Iodide → HCID 11741533, compound

https://huagongshe.com/reaction/2218235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantAcetonitrileHCID 6342—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Azabicyclo[3.1.0]hexane hydrochlorideHCID 22335289—
ReactantHCID 86606011HCID 86606011—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 11741533HCID 11741533—

Reaction Steps

A solution of 3-(2-benzyloxy-5-methylphenyl)-3-phenylpropyl-p-toluene sulphonate (Prepared by following the process as described in EP 0 325 571, 0.486 gm, 1 mmol), 3-azabicyclo[3.1.0]hexane hydrochloride (Prepared by following the process as described in U.S. Pat. No. 4,183,857, 0.12 gm, 1 mmol), potassium carbonate (0.275 gm, 2 mmol), potassium iodide (0.17 gm, 1 mmol) in acetonitrile (10 ml) and dimethylformamide (10 ml) were refluxed for 15 hours at about 100° C. The cooled reaction mixture was poured into water and extracted with ethyl acetate. The combined organic layers were dried over sodium sulphate and concentrated in vacuo to afford an oily residue, which was purified by column chromatography (silica gel 100-200 mesh), eluting the compound with 50-50 ethylacetate-hexane mixture.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07410993B2
Source datasetuspto-grants-2008_08
ORD IDord-23ea20fcb6b746af88da24efbc34ccac
Source noteuspto-grants-2008_08