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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 855196Erstellt: 25. Oktober 2026

Phenethylamine → (4-Tert-butyl-benzyl)-phenethyl-amine

https://huagongshe.com/reaction/855196

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenethylamineHCID 1001—
Edukt4-tert-ButylbenzaldehydeHCID 70324—
EduktSodium borohydrideHCID 4311764—
KatalysatorHydrochloric AcidHCID 313—
LösungsmittelMethanolHCID 887—
Produkt(4-Tert-butyl-benzyl)-phenethyl-amineHCID 455993391,1%

Reaktionsschritte

0.65 ml of 4-tert-butylbenzaldehyde (3.7 mmol) and 0.32 ml of phenethylamine (2.5 mmol) were dissolved in 7.5 ml methanol at rt, and after stirring for 30 min at rt, were refluxed for 2¼ h. After cooling down to rt, 142 mg (3.7 mmol) of sodium borohydride were added and after stirring for 15 min at rt, the reaction mixture was then refluxed for 3.5 h. After cooling down to rt, the reaction mixture was treated with 6 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 609 mg of colorless oil (91%). MS (ISP) 268.3 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07259183B2
Quelldatensatzuspto-grants-2007_08
ORD IDord-2100c4719ff4491f9f7ca0a098534bcc
Quellennotizuspto-grants-2007_08