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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 353600Erstellt: 24. Oktober 2026

4-Chloronaphthylamine → (2-(4-(((4-Chloronaphthyl)amino)methyl)phenoxy)ethyl)diethylamine

https://huagongshe.com/de/reaction/353600

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-ChloronaphthylamineHCID 78408—
Edukt4-(2-(Diethylamino)-Ethoxy)-BenzaldehydeHCID 411674—
EduktSodium borohydrideHCID 4311764—
Katalysatorp-Toluenesulfonic acid monohydrateHCID 521998—
LösungsmittelMethanolHCID 887—
LösungsmittelTolueneHCID 1140—
Produkt(2-(4-(((4-Chloronaphthyl)amino)methyl)phenoxy)ethyl)diethylamineHCID 235143812.089,2%

Reaktionsschritte

A stirred solution of 0.2 gram (0.0001 mole) of 4-(2-(diethylamino)ethoxy)benzaldehyde (prepared in the manner of Step A, Example 3), 0.22 gram (0.0001 mole) of 1-amino-4-chloronaphthalene (available from Aldrich Chemical Company), and one drop of p-toluenesulfonic acid monohydrate (available from Aldrich Chemical Company) in 5 mL of toluene was heated at reflux for ten hours. At the conclusion of this period, the reaction mixture was concentrated under reduced pressure, yielding a residue. The residue was taken up in 5 mL of methanol and about 0.2 grams (0.004 mole) of sodium borohydride was added. The resulting mixture was stirred at ambient temperature for about 18 hours. After this time, the mixture was quenched with water and extracted with several portions of diethyl ether. The extracts were combined, dried with sodium sulfate and filtered. The filtrate was concentrated under reduced pressure, yielding 0.8 gram of Compound 84. The NMR spectrum was consistent with the proposed structure.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06753429B2
Quelldatensatzuspto-grants-2004_06
ORD IDord-ab9d87d4ffa14605a878d926f1c8b7cb
Quellennotizuspto-grants-2004_06