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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345196Generated: October 26, 2026

Toluene → 2-[3-(4,6-Bis-trichloromethyl-s-triazin-2-yl)benzoylmethylene]-3-ethyl-benzothiazoline

https://huagongshe.com/reaction/345196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant3-(4,6-Bis-trichloromethyl-s-triazin-2-yl) benzoylchlorideHCID 14572922—
Reactant3-Ethyl-2-methyl-1,3-benzothiazol-3-ium;4-methylbenzenesulfonic acidHCID 86745138—
SolventTriethylamineHCID 8471—
Product2-[3-(4,6-Bis-trichloromethyl-s-triazin-2-yl)benzoylmethylene]-3-ethyl-benzothiazolineHCID 86745140—

Reaction Steps

3-Ethyl-2-methyl-benzothiazolium-p-toluenesulfonate (5.0 pbw) and 3-(4,6-bis-trichloromethyl-s-triazin-2-yl) benzoylchloride (7.4 pbw) are successively suspended or dissolved, respectively, in 50 pbw of toluene. The mixture is cooled to 15° C. and, at this temperature, 6.0 pbw of triethylamine are added dropwise with the exclusion of moisture. The mixture discolors towards dark brown and is stirred for 3 hours at room temperature. The precipitate that forms is removed by filtration with suction and washed with cold toluene. The residue is digested in 200 pbw of methanol and stirred for about 60 minutes, filtered again and dried. The product is recrystallized from 2-methoxy-ethanol, giving orange-colored crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05055579
Source datasetuspto-grants-1991_10
ORD IDord-844d56ae32684c6a9fc1bb4de4f0426f
Source noteuspto-grants-1991_10