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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 547051Generated: November 2, 2026

Potassium Phosphate, Tribasic → HCID 57709060, compound

https://huagongshe.com/reaction/547051

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantMethyl 2-(4-bromophenyl)acetateHCID 316783—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
ReactantHCID 57709123HCID 57709123—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 57709060HCID 5770906089.7%

Reaction Conditions

Temperature110 °C

Reaction Steps

(4-Bromo-phenyl)acetic acid methyl ester (35 mg, 0.15 mmol), palladium acetate (2.3 mg, 0.01 mmol), 2-dicyclohexylphosphino-2′,6′-dimethoxy-1,1′-biphenyl (8.3 mg, 0.02 mmol), potassium phosphate (65 mg, 0.3 mmol) and water (0.2 mL) were added to a solution of 2-(4-{1-ethyl-1-[3-methyl-4-(4-trimethylsilanyloxy-tetrahydro-thiopyran-4-ylethynyl)-phenyl]-propyl}-2-methyl-phenyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane (Example 136-(4); 60 mg, 0.1 mmol) in toluene (2 mL). The mixture was stirred in a nitrogen atmosphere at 110° C. for two hours. Water was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was purified by silica gel chromatography (hexane:ethyl acetate=1:1) to give the target compound as a colorless oil (55 mg, 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935688B2
Source datasetuspto-grants-2011_05
ORD IDord-d87e1846ea7c4d73b67785152ce049f2
Source noteuspto-grants-2011_05