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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657470Generated: October 26, 2026

Acetic Acid → 2-[(4-Oxo-2-sulfanylidene-1,3-thiazolidin-5-ylidene)methyl]benzoic acid

https://huagongshe.com/reaction/1657470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPhthalaldehydic acidHCID 8406—
ReactantSodium AcetateHCID 517045—
ReactantRhodanineHCID 1201546—
SolventWaterHCID 962—
Product2-[(4-Oxo-2-sulfanylidene-1,3-thiazolidin-5-ylidene)methyl]benzoic acidHCID 2826383—

Reaction Steps

To a hot stirred solution of 20.5 g. (134 mM) of phthalaldehydic acid and 17.95 g. (135 mM) of rhodanine in 90 ml. of glacial acetic acid is added 36.0 g. (438 mM) of sodium acetate. While heating the resulting solution to reflux, a precipitate forms and an additional 30 ml. of acetic acid is added. After refluxing the mixture for 0.5 hour, it is cooled, poured into water, and filtered to separate a yellow solid. The solid is washed with water and boiled with 500 ml. of isopropanol. The resulting mixture is cooled and filtered to separate 31.14 g. (87.5%) of the 5-o-carboxybenzylidenerhodanine as yellow needles, m.p. 276°-278°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03960892
Source datasetuspto-grants-1976_06
ORD IDord-b3ceb61315854b06bea408ebe5657a81
Source noteuspto-grants-1976_06