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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296850Generated: October 25, 2026

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

https://huagongshe.com/reaction/1296850

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChloronaphthylamineHCID 78408—
Reactant4-(2-(Diethylamino)-Ethoxy)-BenzaldehydeHCID 411674—
ReactantSodium borohydrideHCID 4311764—
Catalystp-Toluenesulfonic acid monohydrateHCID 521998—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
Product(2-(4-(((4-Chloronaphthyl)amino)methyl)phenoxy)ethyl)diethylamineHCID 235143812,089.2%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07247756B2
Source datasetuspto-grants-2007_07
ORD IDord-75cb64f9bedf4ead93f4feb3873e1e84
Source noteuspto-grants-2007_07