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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 33726Erstellt: 23. Oktober 2026

Dichloromethane → Ammonia dichloromethane

https://huagongshe.com/de/reaction/33726

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
EduktN-MethylbenzeneethanamineHCID 11503—
EduktSodium HydroxideHCID 14798—
Edukt4-(3-Piperidin-1-ylpropoxy)benzaldehydeHCID 2766324—
EduktSodium triacetoxyborohydrideHCID 5049666—
LösungsmittelAcetic AcidHCID 176—
ProduktMethyl-phenethyl-[4-(3-piperidin-1-yl-propoxy)-benzyl]-amineHCID 10133527—
ProduktAmmonia dichloromethaneHCID 227314291%

Reaktionsschritte

A solution of the product of Example 9 (208 mg), methyl-phenethyl-amine (113 mg), and acetic acid (0.05 mL) in DCM (3 mL) was treated with sodium triacetoxyborohydride (290 mg). After 16 h, the resulting mixture was treated with 10% sodium hydroxide (5 mL) and extracted with DCM (3×10 mL). The combined organic phases were dried (sodium sulfate) and evaporated. Chromatography of the residue (1-5% 2 M methanolic ammonia/DCM) gave the title compound as a colorless oil (300 mg). 1H NMR (400 MHz, CDCl3): 7.30-7.25 (m, 2H), 7.21-7.16 (m, 5H), 6.83 (d, J=8.6 Hz, 2H), 3.99 (t, J=6.3 Hz, 2H), 3.49 (s, 2H), 2.84-2.79 (m, 2H), 2.65-2.62 (m, 2H), 2.51-2.37 (m, 6H), 2.26 (s, 3H), 1.98 (m, 2H), 1.63-1.56 (m, 4H), 1.47-1.40 (m, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07429586B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-4b54ea5fb64f4c08af727180f78627ba
Quellennotizuspto-grants-2008_09