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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2350934Generated: November 2, 2026

Triethylamine → HCID 19847868, compound

https://huagongshe.com/reaction/2350934

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant[2-(Trifluoromethyl)phenyl]hydrazine--hydrogen chloride (1/1)HCID 12891828—
ReactantHCID 19847783HCID 19847783—
SolventTolueneHCID 1140—
ProductHCID 19847868HCID 19847868—

Reaction Steps

A mixture of 6.1 g (22 mmol) of ethyl N-acetyl-2-chloro-4-fluorobenzimidate and 6.7 g (25 mmol) of o-trifluoromethylphenylhydrazine hydrochloride in 100 ml of toluene is treated with 3.9 ml (28 mmol) of triethylamine and the whole is heated at reflux temperature for 18 hours. Thereafter, the reaction mixture is washed once with water and extracted twice with 50 ml of concentrated hydrochloric acid. The acidic aqueous phases are neutralized with ice-cold sodium hydroxide solution and extracted twice with diethyl ether, and the combined extracts are dried over anhydrous magnesium sulfate and evaporated under reduced pressure. The residue is subjected to a bulb-tube distillation, the fractions with b.p. 200° C./0.01 mmHg (9.33 Pa) being collected and finally crystallized from diisopropyl ether/n-hexane. In this manner there is obtained 3-(2-chloro-4-fluorophenyl)-5-methyl-1-(α,α,α-trifluoro-o-tolyl)-1H-1,2,4-triazole, m.p. 116° C.; 1H--NMR (CDCl3, 60 MHz): 2.37 (s,CH3); mass spectrum: 335 (48), 314(43), 159(100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04871757
Source datasetuspto-grants-1989_10
ORD IDord-e6b14690af644817ab80928874e9a3fe
Source noteuspto-grants-1989_10