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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359111Generated: November 1, 2026

Acetic Acid → HCID 21918729, compound

https://huagongshe.com/reaction/1359111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantThioglycolic AcidHCID 1133—
Reactant4-NitroanilineHCID 7475—
Reactant3,5-Di-tert-butyl-4-hydroxybenzaldehydeHCID 73219—
SolventTolueneHCID 1140—
ProductHCID 21918729HCID 2191872914.8%

Reaction Steps

5 g of 3,5-di-t-butyl-4-hydroxybenzaldehyde (21 mmol) and 2.95 g of para-nitroaniline (21 mmol) are dissolved in 50 ml of anhydrous toluene. 0.5 ml of glacial acetic acid is added and the whole is taken to reflux for 24 hours. Then 1.96 g of mercaptoacetic acid (21 mmol) is added to the medium and reflux is continued for another 24 hours. After the reaction mixture has returned to ambient temperature, it is washed with water (3 times 30 ml). After decantation. the organic phase is dried over sodium sulphate and the solvent is evaporated off under reduced pressure. The residue is purified on silica gel in an ethyl acetate/heptane mixture (1/4) and 1.33 g of pure 2-(3,5-di-t-butyl-4-hydroxyphenyl)-3-(4-nitrophenyl)-4-thiazolidinone is obtained in the form of a colourless oil (15%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06599903B2
Source datasetuspto-grants-2003_07
ORD IDord-b064aa7b0a6c4cc49f5a713868c9d610
Source noteuspto-grants-2003_07