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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 855271Erstellt: 25. Oktober 2026

Phenethylamine, m-trifluoromethyl- → [4-(1-Methylcyclopropyl)-benzyl]-[2-(3-trifluoromethylphenyl)-ethyl]-amine

https://huagongshe.com/reaction/855271

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenethylamine, m-trifluoromethyl-HCID 104223—
EduktSodium borohydrideHCID 4311764—
Edukt(4-Cyclopropylbenzyl)-[2-(4-fluoro-3-trifluoromethylphenyl)-ethyl]-amineHCID 69342889—
Edukt4-(1-Methylcyclopropyl)benzaldehydeHCID 86093847—
Produkt[4-(1-Methylcyclopropyl)-benzyl]-[2-(3-trifluoromethylphenyl)-ethyl]-amineHCID 6934273862%

Reaktionsschritte

The title compound was synthesized in analogy to (4-cyclopropylbenzyl)-[2-(4-fluoro-3-trifluoromethylphenyl)-ethyl]-amine (described in example S53) using 4-(1-methyl-cyclo-propyl)-benzaldehyde (150 mg, 0.94 mmol), 2-(3-trifluoromethylphenyl)-ethylamine (177 mg, 0.94 mmol) and sodium borohydride (53 mg, 1.40 mmol). The isolated residue was purified by flash column chromatography (2%-5% MeOH in EtOAc) to give the desired product (195 mg, 62%) as a colorless oil. MS (ISP) 334.3 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07259183B2
Quelldatensatzuspto-grants-2007_08
ORD IDord-68755597b46146b0a46321230ff37374
Quellennotizuspto-grants-2007_08