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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 882333Generated: October 27, 2026

4-Fluorobenzaldehyde → N-(4-fluorobenzyl)-N-[(trans)-2-phenylcyclopropyl]amine

https://huagongshe.com/reaction/882333

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorobenzaldehydeHCID 68023—
ReactantTranylcypromine hydrochlorideHCID 2723716—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductN-(4-fluorobenzyl)-N-[(trans)-2-phenylcyclopropyl]amineHCID 4686973449.7%

Reaction Steps

A mixture of (trans)-2-phenylcyclopropanamine hydrochloride (0.25 g, 1.50 mmol) and 4-fluorobenzaldehyde (0.18 mL, 1.65 mmol) in CH2Cl2 (8 mL) and water (0.5 mL) was vigorously stirred at room temperature for 10 min. Then, NaBH(OAc)3 (0.41 g, 1.95 mmol) was slowly added and stirring continued for 1.5 h. The reaction mixture was washed with an aqueous saturated solution of NaHCO3 (10 mL), the organic layer was dried over anhydrous Na2SO4, filtered and, after removal of the solvent, the residual oil was purified by column chromatography on silica gel (3% MeOH/CH2Cl2) affording 0.18 g of N-(4-fluorobenzyl)-N-[(trans)-2-phenylcyclopropyl]amine [Rf=0.5 (5% MeOH/CH2Cl2), colorless oil, 49% yield].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993808B2
Source datasetuspto-grants-2015_03
ORD IDord-ef3aa42e11e041048a0777e3ae607b4e
Source noteuspto-grants-2015_03