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HRID 19781Erstellt: 23. Oktober 2026

4-tert-Butylbenzaldehyde → (4-Tert-butylbenzyl)-[2-(3,4-dichloro-phenyl)-ethyl]-amine

https://huagongshe.com/de/reaction/19781

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-tert-ButylbenzaldehydeHCID 70324—
Edukt3,4-DichlorophenethylamineHCID 217958—
EduktSodium borohydrideHCID 4311764—
KatalysatorHydrochloric AcidHCID 313—
LösungsmittelMethanolHCID 887—
Produkt(4-Tert-butylbenzyl)-[2-(3,4-dichloro-phenyl)-ethyl]-amineHCID 68563688102,1%

Reaktionsschritte

0.38 ml of 4-tert-butylbenzaldehyde (2.25 mmol) and 0.227 ml 2-(3,4-dichloro-phenyl)-ethylamine (1.5 mmol) were dissolved in 4.5 ml methanol at RT, and after stirring for 30 min at RT, were refluxed for 2 h. After cooling down to RT, 85 mg (2.25 mmol) sodium borohydride were added and after stirring for 5 min at RT, the reaction mixture was then refluxed for 2 h. After cooling down to RT, the reaction mixture was treated with 4 drops 1 N HCl and concentrated in vacuo. The residue was diluted with water/EtOAc. After separation of the organic phase, the aqueous phase was extracted with EtOAc and the combined organic phases were washed with brine, dried with magnesium sulfate, filtered off and concentrated in vacuo. The residue was purified by column chromatography (40 g silica gel; EtOAc/heptane 1:2) to give 515 mg colorless viscous oil (97%). MS (ISP) 336.2 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745477B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-a189fa60b3d0427fa29e1260ede59189
Quellennotizuspto-grants-2010_06