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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416008Generated: October 31, 2026

Triethylamine → HCID 22637223, compound

https://huagongshe.com/reaction/2416008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant(2-Nitrophenyl)acetic acidHCID 77337—
Reactant1-[3-Chloro-5-(trifluoromethyl)pyridin-2-yl]methanamine hydrochlorideHCID 11499744—
SolventTolueneHCID 1140—
ProductHCID 22637223HCID 22637223—

Reaction Steps

To a stirred suspension of 2-nitrophenylacetic acid (0.36 g) in dry toluene (5 ml) at room temperature was added phosphoryl chloride (0.37 g) and stirring was continued overnight. Meanwhile a solution of the amine was prepared, (3-Chloro-5-trifluoromethyl-2-pyridyl)methylamine hydrochloride (0.49 g) in dry toluene (5 ml) and triethylamine (1.23 g) was stirred at room temperature for 1 hour and then filtered. The solid was washed with dry toluene and the combined filtrates were added dropwise to the above suspension of acid chloride with ice-cooling. After addition, the mixture was stirred at room temperature overnight. Dichloromethane was added and the mixture was washed with water. The aqueous layer was separated and back-extracted with dichloromethane. The combined organic extracts were washed with saturated sodium bicarbonate solution, then brine, then dried (MgSO4), and the solvent removed. The resulting residue was purified by silica gel chromatography eluting with ethyl acetate/light petroleum (b.p. 40-60° C.) to give the title product, m.p. 123-4° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06821992B1
Source datasetuspto-grants-2004_11
ORD IDord-330dbff2af3d491fbbd72c30ecbd6c82
Source noteuspto-grants-2004_11