HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 735950Generated: October 29, 2026
2-(2-Fluorophenyl)ethylamine → N-[2-(2-fluorophenyl)ethyl]-N-[4-(3-undecyl-1,2,4-oxadiazol-5-yl)benzyl]amine
https://huagongshe.com/reaction/735950
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(2-Fluorophenyl)ethylamine | HCID 643357 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 4-(3-Undecyl-1,2,4-oxadiazol-5-yl)benzaldehyde | HCID 86598531 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[2-(2-fluorophenyl)ethyl]-N-[4-(3-undecyl-1,2,4-oxadiazol-5-yl)benzyl]amine | HCID 67187358 | — |
Reaction Steps
To a solution of 4-(3-undecyl-1,2,4-oxadiazol-5-yl)benzaldehyde (32.8 mg, 0.1 mmol) in anhydrous THF (0.6 mL) was added the 2-(2-fluorophenyl)ethylamine (11.8 mg, 0.1 mmol) and Ti(iPrO)4 (0.035 mL, 0.12 mmol). The mixture was stirred for 3 h at 60° C. then sodium triacetoxyborohydride (53 mg, 0.25 mmol) was added and the reaction mixture was stirred overnight at rt. THF (0.75 mL) was added followed by the PS-DEAM resin (Argonaut, 148 mg, 1.68 mmol/g), and the reaction mixture was stirred at rt overnight. The reaction mixture was filtered and the filtrates were eluted through a SCX column (Isolute, 1 g) with DCM (6 mL), then NH3 (2M in MeOH, 4 mL). The desired fractions (TLC monitoring) were concentrated under vacuum to give the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07592477B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-6a207b370cc54f93880620dbf7789bba |
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| Source note | uspto-grants-2009_09 |
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