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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855311Generated: November 3, 2026

Potassium Carbonate → HCID 86711700, compound

https://huagongshe.com/reaction/1855311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactantethyl (2R)-5-oxopyrrolidine-2-carboxylateHCID 643508—
ReactantHCID 11383144HCID 11383144—
SolventAcetonitrileHCID 6342—
SolventN,N'-DimethylethylenediamineHCID 8070—
SolventCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
ProductHCID 86711700HCID 86711700—

Reaction Conditions

Temperature23 °C

Reaction Steps

To a flask containing acetonitrile was added [(S)-1-(4-bromo-phenyl)-hexyloxy]-tert-butyl-dimethyl-silane and potassium carbonate. The solution mixture was heated to reflux for a period of time. The solution mixture was then cooled to ambient temperature (˜23° C.) before adding a solution of (R)-5-oxo-pyrrolidine-2-carboxylic acid ethyl ester in acetonitrile, CuI and N,N′-dimethylethylenediamine. The reaction mixture was heated to reflux until the ethyl ester was consumed. The reaction mixture was cooled to ambient temperature, filtered through a bed of Celite and rinsed forward with acetonitrile. The filtrate was washed twice with aqueous ammonium acetate and dried over sodium sulfate. The mixture was passed through a bed of silica, washed with MTBE, and concentrated under reduced pressure to give the product as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962863B2
Source datasetuspto-grants-2015_02
ORD IDord-5f5a55ccd808439b918b0ecab5ef556b
Source noteuspto-grants-2015_02