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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2293970Generated: October 31, 2026

Pyridine → 2-(4-Fluorophenyl)-1-phenylethan-1-amine

https://huagongshe.com/reaction/2293970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthyl AcetateHCID 8857—
ReactantBorane;tetrahydrofuranHCID 2723981—
ReactantHCID 54455826HCID 54455826—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Fluorophenyl)-1-phenylethan-1-amineHCID 1500897766%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 2-(4-fluorophenyl)-1-phenyl-1-ethanone-O-methyl oxime (1.34 g, 4.62 mmol) in 30 ml dry THF under nitrogen was added borane-THF complex (1.0M in THF, 23.1 ml, 23.1 mmol) and dry pyridine (10 ml) by syringe at 25° C. The resulting bi-phasic solution was refluxed with vigorous magnetic stirring for 16 hours. After the reaction was cooled to 25° C. and was quenched with 10% NaOH solution, hexanes (50 ml) were added and the layers were separated. The aqueous portion was extracted with hexanes again (40 ml). The combined organic layers were dried over magnesium sulfate and concentrated in vacuo to yield a cloudy colorless syrup (3.55 g, 66% yield for two steps). Rf : 0.24 (EtOAc).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05688789
Source datasetuspto-grants-1997_11
ORD IDord-d9f4d4017545483bba7f565631882877
Source noteuspto-grants-1997_11