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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811501Generated: October 30, 2026

Potassium Phosphate, Tribasic → HCID 58065892, compound

https://huagongshe.com/reaction/1811501

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTricyclohexylphosphineHCID 75806—
ReactantCyclopropylboronic acidHCID 2760897—
ReactantHCID 58065882HCID 58065882—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 58065892HCID 58065892—

Reaction Conditions

Temperature100 °C

Reaction Steps

Following a literature procedure (Petit, S; Duroc, Y; Larue, V; Giglione, C; Leon, C; Soulama, C; Denis, A; Dardel, F; Meinnel, T; Artaud, I. ChemMedChem 2009, 4, 261-275), tert-butyl 3,6-dibromo-9H-carbazole-9-carboxylate (0.0200 g, 0.0470 mmol), cyclopropyl boronic acid (0.0202 g, 0.235 mmol), palladium acetate (10 mol %, 0.0011 g, 0.00470 mmol), potassium phosphate tribasic (0.0350 g, 0.165 mmol), tricyclohexylphosphine (0.0026 g, 0.00941 mmol), water (12.2 μL) and a stir bar were combined in a sealed vial. The vial was sparged with N2 and charged with 0.22 mL degassed toluene. The mixture was stirred at 100° C. for 65 h. The crude reaction mixture was diluted with 10 mL EtOAc and washed with brine (3×10 mL). The organic layer was dried over anhydrous Na2SO4 and evaporated to afford the crude product, which was used as is without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362277B2
Source datasetuspto-grants-2013_01
ORD IDord-5dba09d836fd4a59b01d50b23cb682a5
Source noteuspto-grants-2013_01