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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075127Generated: November 2, 2026

Potassium Carbonate → HCID 66916938, compound

https://huagongshe.com/reaction/2075127

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(3-Chlorophenyl)boronic acidHCID 2734323—
Reactant(4-Bromophenyl)(piperidin-4-yl)methanoneHCID 13180300—
CatalystPalladiumHCID 23938—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
ProductHCID 66916938HCID 6691693890.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

A round bottom flask was charged with (4-bromophenyl)(piperidine-4-yl)methanone (20.0 g, 74.6 mmol), 3-chlorophenyl boronic acid (17.4 g, 111 mmol, 1.5 eq), and palladium encapsulated catalyst (Aldrich, Pd EnCat-TPP®, catalyst species PdCl2(PPh3)2) (5.2 g, 0.187 mmol, 0.05 eq). These solids were suspended in isopropanol (570 ml) and allowed to stir for five minutes. To the mixture was added potassium carbonate (30.8 g, 224 mmol, 3 eq) dissolved in H2O (30 ml). The reaction mixture was heated to 80° C. for 16 hours and deemed complete by LC/MS. The suspension was filtered through a small bed of Celite® and the filtrate was concentrated to dryness. The resulting solids were dissolved in isopropyl acetate (400 ml) and washed with water (3×75 ml). The organic layer was then cooled to 0° C. (ice/water bath) and to this stirring solution was added slowly 6 N HCl until solids crystallized. The solids were filtered and dried in a vacuum oven for 16 hours at 50° C. to afford 16.9 g of compound 2 (68% yield) in >98% HPLC purity. MH+=300, 302 (about 3:1). Palladium: 3 ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919618B2
Source datasetuspto-grants-2011_04
ORD IDord-b24d2ab1794a460382f196974ce5c0f3
Source noteuspto-grants-2011_04