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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822178Generated: October 25, 2026

Pyridine → 2-[(3-Chloro-4-fluorophenyl)(1-phenylethyl)amino]propan-1-ol

https://huagongshe.com/reaction/1822178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant3-Chloro-4-fluorophenylboronic Acid (contains varying amounts of Anhydride)HCID 2734660—
Reactant2-[(1-Phenylethyl)amino]propan-1-olHCID 43499692—
CatalystCupric acetateHCID 8895—
SolventDichloromethaneHCID 6344—
Product2-[(3-Chloro-4-fluorophenyl)(1-phenylethyl)amino]propan-1-olHCID 11688120—

Reaction Steps

2-[(1-phenylethyl)amino]propan-1-ol (5-5, 0.027 g, 0.151 mmol) in CH2Cl2 (1.0 mL) was treated with Cu(OAc)2 (0.041 g, 0.227 mmol), pyridine (0.024 mL, 0.302 mmol), and 4-fluoro-3-chloro-phenylboronic acid (0.026 g, 0.149 mmol). 4 A MS (20 mg) were added and the resulting solution stirred 24 h. Upon completion, the reaction mixture was filtered and the filtrate was purified by reverse phase liquid chromatography (Semi-prep YMC C-18 Column 5% CH3CN/H2O up to 95% CH3CN/H2O) to give 2-[(3-chloro-4-fluorophenyl)(1-phenylethyl)amino]propan-1-ol (5-6) as a brown oil. MS 308.3 found 308.8 (M+H+) required.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608739B2
Source datasetuspto-grants-2009_10
ORD IDord-7ec9d61050d0421da0e885be2358903a
Source noteuspto-grants-2009_10