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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 986380Generated: October 30, 2026

Acetonitrile → p-Toluenesulfonic acid

https://huagongshe.com/reaction/986380

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantHCID 13796806HCID 13796806—
ReactantHCID 73186994HCID 73186994—
SolventTriethylamineHCID 8471—
Productp-Toluenesulfonic acidHCID 6101211.5%

Reaction Steps

5.2 g of 5-chloro-3-ethyl-2-{(4-methyl-2H-chromen-2-ylidene)methyl}-benzothiazolium p-toluenesulfonate and 4.3 g of 5-chloro-3-ethyl-2-ethylthiobenzothiazolium p-toluenesulfonate were added to 140 ml of acetonitrile and dissolved under heat, and then 4.5 ml of triethylamine was added thereto and reacted for 5 minutes. After cooling the precipitated crystals were separated by filtration and recrystallized from a mixed solvent of methanol/chloroform, to obtain 3.6 g of the desired p-toluenesulfonate product. Yield: 50%. Appearance: Brilliant brown crystal. M.p.: above 240° C. (decomposition). ##STR11##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04713316
Source datasetuspto-grants-1987_12
ORD IDord-90ebf661d4c44964aea67b2bf5a4aba0
Source noteuspto-grants-1987_12