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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 986376Generated: October 25, 2026

Acetone → 3-Ethyl-2-{(4-methyl-2H-chromen-2-ylidene)methyl}-benzothiazolium perchlorate

https://huagongshe.com/reaction/986376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantMethanolHCID 887—
ReactantPerchloric AcidHCID 24247—
Reactant3-Ethyl-2-methyl-1,3-benzothiazol-3-ium;4-methylbenzenesulfonic acidHCID 86745138—
Product3-Ethyl-2-{(4-methyl-2H-chromen-2-ylidene)methyl}-benzothiazolium perchlorateHCID 13171541840%

Reaction Conditions

Temperature150 °C

Reaction Steps

17.5 g of 3-ethyl-2-methylbenzothiazolium-p-toluenesulfonate and 8.8 g of 4-methylcoumarin-2-thione were reacted under heat at 150° C. for 15 hours, and 20 ml of methanol and 40 ml of acetone were then added to the reaction mixture in the order listed to obtaina uniform solution. After cooling to room temperature, 15.7 g of 60%-perchloric acid was added thereto and stirred at room temperature, whereby crystals precipitated out. The crystals formed were filtered out and washed with a small amount of acetone, and thereafter the crystals were placed in a mixed solvent comprising 20 ml of methanol and 40 ml of acetone at room temperature and stirred for 30 minutes. Then the crystals were again separated by filtration and washed with acetone, to finally obtain 8.5 g of the desired perchlorate product. Yield: 40%. Appearance: brown crystal. M.p.: above 280° C. (decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04713316
Source datasetuspto-grants-1987_12
ORD IDord-2c969d06f7544bb788aa32466123cb33
Source noteuspto-grants-1987_12