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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566552Generated: October 27, 2026

Potassium Iodide → HCID 54307972, compound

https://huagongshe.com/reaction/566552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantPotassium CarbonateHCID 11430—
Reactantethyl (3R)-piperidine-3-carboxylateHCID 185582—
Reactant3-(3,3-Bis(2-methylphenyl)-2-propen-1-yloxy)-1-propanolHCID 10756363—
ReactantButyllithiumHCID 178418339—
SolventAcetoneHCID 180—
SolventTolueneHCID 1140—
ProductHCID 54307972HCID 5430797252%

Reaction Steps

A solution of 3-(3,3-bis(2-methylphenyl)-2-propen-1-yloxy)-1-propanol (3.45 g, 11.6 mmol) in dry toluene (150 ml) was cooled in an ice-bath and a solution of n-butyllithium in hexanes (5.1 ml, 2.5 M) was added dropwise. The reaction mixture was stirred for 15 minutes at room temperature and p-toluenesulphonyl chloride (2.44 g, 12.8 mmol) was added. The mixture was stirred at room temperature for 3 h. Ethyl (R)-3-piperidinecarboxylate (4.5 g, 23.3 mmol) and potassium carbonate (3.2 g, 23.3 mmol) were added and the mixture was stirred at room temperature for 0.5 h and then at 75° C. for 12 h. Potassium iodide (1.0 g) and acetone (40 ml) were added and the mixture was heated at reflux temperature for 15 h. Acetone (50 ml) was added and the cooled reaction mixture was filtered and the solvent evaporated in vacuo. Flash chromatography of the residue on silica gel (280 g) using a gradient of n-heptane in ethyl acetate as eluent afforded 2.6 g (52%) of (R)-N-(3-(3,3-bis-(2-methylphenyl)-2-propen-1-yloxy)-1-propyl)-3-piperidinecarboxylic acid ethyl ester as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06174898B1
Source datasetuspto-grants-2001_01
ORD IDord-3fea8c6960184161874254faa2e5a54d
Source noteuspto-grants-2001_01