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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248407Generated: October 27, 2026

Triethylamine → 4-Fluoro-alpha-(2-[2-(2-naphthalenyl)ethylamino]ethyl)benzenemethanamine Dihydrochloride

https://huagongshe.com/reaction/2248407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Chloro-4'-fluoropropiophenoneHCID 67672—
Reactant2-(Naphthalen-2-yl)ethan-1-amine hydrochlorideHCID 16218122—
SolventTetrahydrofuranHCID 8028—
Product4-Fluoro-alpha-(2-[2-(2-naphthalenyl)ethylamino]ethyl)benzenemethanamine DihydrochlorideHCID 19996145—

Reaction Steps

A solution of 3-chloro-4'-fluoropropiophenone (9.3 g, 0.05 mole) in 100 ml THF was treated with triethylamine (5.6 g, 0.055 mole) and stirred at room temperature for one hour. The mixture was treated with 2-naphthaleneethylamine hydrochloride (10.4 g, 0.05 mole) and refluxed for six hours. The reaction mixture was cooled to room temperature, and the resulting crystals were collected by filtration, washed with THF, ether, and water; and dried to give the title compound as a homogeneous product by tlc (chloroform-methanol, 9:1) (96%, 17.2 g); mp 208°-210° C.; IR(nujol): C=O @ 1675 cm-1 ; NMR(DMSO-d6, TMS): δ 3.20(t,2H, CH2 --CO), 3.37(m,4H,Ar--CH2 --CH2), 3.60(t,2H,N--CH2) [7.3-7.6(m,5H), 7.7-7.8(m,2H), 8.10(m,2H) aromatic]; Anal. Found: C,70.37; H,5.92; N,3.81. Mass spectrum m/e 321,184.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05039706
Source datasetuspto-grants-1991_08
ORD IDord-b8e07242d60149519281ecaf6939d085
Source noteuspto-grants-1991_08