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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Reactant | HCID 54455826 | HCID 54455826 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(4-Fluorophenyl)-1-phenylethan-1-amine | HCID 15008977 | 66% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05688789 |
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| Source dataset | uspto-grants-1997_11 |
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| ORD ID | ord-d9f4d4017545483bba7f565631882877 |
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| Source note | uspto-grants-1997_11 |
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