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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705842Generated: November 1, 2026

Ammonia → 3-(4-(4-Chloro-3-(trifluoromethyl)phenoxy)phenyl)propanimidamide

https://huagongshe.com/reaction/705842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantAcetyl chlorideHCID 6367—
Reactant3-(4-(4-Chloro-3-(trifluoromethyl)phenoxy)phenyl)propanenitrileHCID 67773517—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
Product3-(4-(4-Chloro-3-(trifluoromethyl)phenoxy)phenyl)propanimidamideHCID 6777563973%

Reaction Steps

To a solution of 3-(4-(4-chloro-3-(trifluoromethyl)phenoxy)phenyl)propanenitrile (1 g, 3.07 mmol) in toluene (4 mL) and methanol (1 mL) was added dropwise AcCl (1.091 mL, 15.35 mmol) at 0° C. in 5 min. The mixture was stirred at room temperature for 2 h. The mixture was cooled to 0° C. in an ice bath, and ammonia (4.39 mL, 30.7 mmol) in methanol was added dropwise in 5 min. The mixture was stirred at room temperature overnight. The mixture was filtered to remove the solid, and the solid was washed with toluene (20 mL) and methanol (20 mL). The combined filtrate was concentrated in vacuo, the residue was triturated with diethyl ether, the resulting white solid was collected by filtration, washed with diethyl ether and dried in vacuo to afford the title compound (0.85 g, 2.242 mmol, 73.0% yield) as white solid. LCMS: rt=1.17 min, [M+H+]=343

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174968B2
Source datasetuspto-grants-2015_11
ORD IDord-ea327b3cb552464da8df5251d7e4522b
Source noteuspto-grants-2015_11