HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 560552Generated: October 28, 2026
p-Fluorophenethylamine → N-(4-fluorophenethyl)-2,2-dimethoxyethanamine
https://huagongshe.com/reaction/560552
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Fluorophenethylamine | HCID 4653 | — |
| Reactant | Acetaldehyde, 2,2-dimethoxy- | HCID 162650 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(4-fluorophenethyl)-2,2-dimethoxyethanamine | HCID 63686615 | 52% |
Reaction Steps
To a solution of 4-fluorophenethylamine (2.00 mL, 15.0 mmol) and dimethoxyacetaldehyde (60% solution in water, 2.53 mL, 16.83 mmol) in tetrahydrofuran (100 mL) was added sodium triacetoxyborohydride (4.28 g, 20.20 mmol) at ambient temperature. The resulting reaction mixture was stirred at ambient temperature for 16 hours. The reaction was quenched by the addition of saturated sodium bicarbonate (50 mL). The mixture was extracted with ethyl acetate (3×100 mL) and the combined organic solution was dried over anhydrous sodium sulfate, filtered, and concentrated. The residue was purified by column chromatography eluted with ethyl acetate/hexane to afford N-(4-fluorophenethyl)-2,2-dimethoxyethanamine as a colorless oil in 52% yield (1.78 g): 1H NMR (300 MHz, CDCl3) δ 7.14-7.10 (m, 2H), 6.97-6.91 (m, 2H), 4.43-4.40 (m, 1H), 3.35 (s, 6H), 2.89-2.81 (m, 2H), 2.76-2.71 (m, 4H); MS (ES+) m/z 228.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063084B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-5aa3e61ea99843c5a6e0e9221e786e31 |
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| Source note | uspto-grants-2011_11 |
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