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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093309Generated: November 1, 2026

Cesium carbonate → HCID 66593802, compound

https://huagongshe.com/reaction/1093309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Reactant1,1-Dimethylethyl N-(5-ethynyl-2,2-dimethyl-1,3-dioxan-5-yl)carbamateHCID 11514385—
ReactantHCID 59407692HCID 59407692—
CatalystBis(acetonitrile)dichloropalladiumHCID 6093782—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 66593802HCID 66593802—

Reaction Steps

Compound 2-1 (0.544 g), (5-ethynyl-2,2-dimethyl-1,3-dioxan-5-yl)carbamic acid t-butyl ester (0.459 g), 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl (0.36 g), bis(acetonitrile)palladium(II) dichloride (0.007 g) and cesium carbonate (0.538 g) were stirred in acetonitrile (8.3 ml) at 70-80° C. for 2 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate, washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography to give (5-{2-[3-cyano-4-(4-phenylbutoxy)phenyl]ethynyl}-2,2-dimethyl-1,3-dioxan-5-yl)carbamic acid t-butyl ester as a yellow oil. This oil was dissolved in ethyl acetate (6 ml), 10% palladium carbon (containing water about 50%, 0.080 g) was added, and the mixture was stirred under a hydrogen atmosphere at room temperature for 3.5 hr. The solution was filtered, and the filtrate was concentrated to give the object product (0.519 g) as a pale-yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129361B2
Source datasetuspto-grants-2012_03
ORD IDord-41b43d7d07c444b2ad9cb3b060761b74
Source noteuspto-grants-2012_03