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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 882337Generated: November 1, 2026

4-(Trifluoromethyl)benzaldehyde → HCID 46869801, compound

https://huagongshe.com/reaction/882337

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)benzaldehydeHCID 67996—
ReactantTranylcypromine hydrochlorideHCID 2723716—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 46869801HCID 4686980138%

Reaction Steps

A mixture of (trans)-2-phenylcyclopropanamine hydrochloride (0.23 g, 1.36 mmol) and 4-(trifluoromethyl)benzaldehyde (0.20 mL, 1.49 mmol) in CH2Cl2 (8 mL) and water (0.5 mL) was vigorously stirred at room temperature for 10 min. Then, NaBH(OAc)3 (0.37 g, 1.76 mmol) was slowly added and stirring continued for 30 min. The reaction mixture was washed with an aqueous saturated solution of NaHCO3 (8 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 (1% MeOH/CH2Cl2) affording 0.15 g of N-[(trans)-2-phenylcyclopropyl]-N-[4-(trifluoromethyl)benzyl]amine [Rf=0.6 (5% MeOH/CH2Cl2), colorless oil, 38% yield].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993808B2
Source datasetuspto-grants-2015_03
ORD IDord-66d7fbcb5c384fe09bc71cb43594ef34
Source noteuspto-grants-2015_03