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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187689Generated: November 1, 2026

2-(Di-tert-butylphosphino)biphenyl → HCID 86659386, compound

https://huagongshe.com/reaction/1187689

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Di-tert-butylphosphino)biphenylHCID 2734215—
Reactant(S)-1-(4-Fluorophenyl)-ethylamineHCID 2779063—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 86659387HCID 86659387—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 86659386HCID 8665938653.9%

Reaction Conditions

Temperature85 °C

Reaction Steps

100 mg of 2,6-dichloro-4-(1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-pyrazol-4-yl)pyridine obtained by Step 2, 44 mg of (S)-(−)-1-(4-fluorophenyl)ethylamine, 17 mg of 2-(di-t-butylphosphino)biphenyl, 70 mg of sodium t-butoxide and 6 mg of palladium acetate were added in turn to 3 ml of degassed toluene, and then the mixture was stirred at 85° C. for 1.5 hours under argon atmosphere. The reaction solution was diluted with ethyl acetate. The solution was washed in turn with water and brine and then dried over magnesium sulfate. The solvent was distilled off under reduced pressure, and then the obtained residue was purified by silica gel column chromatography to obtain 70 mg of the objective compound as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673891B2
Source datasetuspto-grants-2014_03
ORD IDord-36a83bbf24c64401878c124db1ccd4f4
Source noteuspto-grants-2014_03