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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269538Generated: November 2, 2026

Potassium Iodide → HCID 9846282, compound

https://huagongshe.com/reaction/2269538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(4-Chlorophenyl)-4-hydroxypiperidineHCID 38282—
Reactant5-(3-bromopropylidene)-10,11-dihydro-5H-dibenzo[a,d]cyclohepteneHCID 1712685—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 9846282HCID 984628288.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 5-(3-bromopropylidene)-10,11-dihydro-5H-dibenzo[a,d]cycloheptene (described in JP 48-030064)(200 mg) in DMF (10 ml) were added 4-(4-chlorophenyl)-4-hydroxypiperidine (230 mg), potassium carbonate (360 mg), and potassium iodide (50 mg). The mixture was stirred at 70° C. for 24 hours. Water and ethyl acetate were added to the reaction mixture, the organic layer was separated and washed with saturated aqueous sodium chloride, and dried with magnesium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography eluting with ethyl acetate-hexane (1:1) to give the titled compound (250 mg) . 1H-NMR (CDCl3) δ: 1.65-2.11 (5H,m) , 2.32-3.10 (8H,m), 3.22-3.67(4H,m), 5.87(1H,t), 7.03-7.44(12H,m). MS m/z: 444(M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329385B1
Source datasetuspto-grants-2001_12
ORD IDord-8b770451cb774cfcaf649f99b3b2869f
Source noteuspto-grants-2001_12