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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655045Generated: October 25, 2026

Acetic Acid → HCID 178425411, compound

https://huagongshe.com/reaction/1655045

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantChlorineHCID 24526—
Reactant2,6-Dichloro-3-methylanilineHCID 116529—
ReactantHCID 178474478HCID 178474478—
ProductHCID 178425411HCID 178425411—

Reaction Conditions

Temperature15 °C

Reaction Steps

5-Acetylamino-3-mercapto-1,2,4-triazole (15.6 g, 0.10 mole) was added to 250 ml of acetic acid containing 3.6 g (0.20 mole) of water. The mixture was cooled to 15° C. with an external ice bath and 21 g (0.30 mole) of chlorine was added as a gas under the surface of the liquid with stirring over a 30 min. period. About 200 ml of volatiles were then removed from the mixture by evaporation under reduced pressure at up to 120° C. The residue was combined with 17.6 g (0.10 mole) of 2,6-dichloro-3-methylaniline and the mixture heated with stirring at 115° C. for 9 hours. A 100 ml portion of water and 25 ml of concentrated aqueous hydrochloric acid were added and the mixture heated at reflux for 12 hours. It was then allowed to cool and the solids present were collected by filtration. The solids were then placed in 200 ml of 10 percent aqueous sodium hydroxide and the insoluble fraction removed by filtration. The filtrate was acidfied with aqueous hydrochloric acid to pH 4.5 and the solids that formed were recovered by filtration and dried under reduced pressure to obtain 8.9 g (20 percent of theory) of the title compound assaying 80 percent purity by high pressure liquid chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05410065
Source datasetuspto-grants-1995_04
ORD IDord-6fe7cf8e995e40a28819b89c4f3bd46e
Source noteuspto-grants-1995_04