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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 855207Erstellt: 25. Oktober 2026

4-tert-Butylbenzaldehyde → [Rac]-(4-tert-butyl-benzyl)-[2-(4-chloro-phenyl)-2-hydroxy-ethyl]-amine

https://huagongshe.com/reaction/855207

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-tert-ButylbenzaldehydeHCID 70324—
Edukt2-Amino-1-(4-chlorophenyl)ethan-1-olHCID 412434—
EduktSodium borohydrideHCID 4311764—
LösungsmittelMethanolHCID 887—
LösungsmittelWater ethylacetateHCID 22728543—
Produkt[Rac]-(4-tert-butyl-benzyl)-[2-(4-chloro-phenyl)-2-hydroxy-ethyl]-amineHCID 69342320—

Reaktionsschritte

1 ml of 4-tert-butylbenzaldehyde (6.15 mmol) and 960 mg of [rac]-2-amino-1-(4-chloro -phenyl)-ethanol (estimated 4.1 mmol) were dissolved in 40 ml methanol at rt, and after stirring for 5 min at rt, were refluxed for 2 h. After cooling down to rt, 310 mg (8.2 mmol) of sodium borohydride were added and after stirring for 15 min at rt, the reaction mixture was then refluxed for 2 h. After cooling down to rt, 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 stirred with a small quantity of diethylether/heptane, filtered and the solid dried under high vacuo, leading to 723 g of [rac]-(4-tert-butyl-benzyl)-[2-(4-chloro-phenyl)-2-hydroxy-ethyl]-amine as a white solid (55%). MS (ISP) 318.2 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07259183B2
Quelldatensatzuspto-grants-2007_08
ORD IDord-639939a6e94546d8a4bbb53f9d41552b
Quellennotizuspto-grants-2007_08