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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-Fluorophenyl)ethylamineHCID 643357—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-(3-Undecyl-1,2,4-oxadiazol-5-yl)benzaldehydeHCID 86598531—
SolventTetrahydrofuranHCID 8028—
ProductN-[2-(2-fluorophenyl)ethyl]-N-[4-(3-undecyl-1,2,4-oxadiazol-5-yl)benzyl]amineHCID 67187358—

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592477B2
Source datasetuspto-grants-2009_09
ORD IDord-6a207b370cc54f93880620dbf7789bba
Source noteuspto-grants-2009_09