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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660122Generated: October 29, 2026

2,4-Pentadienoic acid, (2E)- → 5-carboxy-2,3,5,8-tetrahydro-1,3-dioxo-1H-1,2,4-triazolo[1,2-a]pyridazine-2-acetic acid

https://huagongshe.com/reaction/1660122

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Pentadienoic acid, (2E)-HCID 95516—
ReactantTert-Butyl hypochloriteHCID 521297—
Reactant2-(3,5-Dioxo-1,2,4-triazolidin-4-yl)acetic acidHCID 20557530—
Solvent1,4-DioxaneHCID 31275—
Product5-carboxy-2,3,5,8-tetrahydro-1,3-dioxo-1H-1,2,4-triazolo[1,2-a]pyridazine-2-acetic acidHCID 2055751543%

Reaction Steps

1.69 g (0.011 mol) of 3,5-dioxo-1,2,4-triazolidine-4-acetic acid were suspended in 20 ml of dry dioxan and the suspension was stirred at room temperature under a stream of nitrogen. A solution of 1.32 g (0.012 mol) of tert.butyl hypochlorite in 4 ml of dry dioxan was added dropwise over a period of 15 minutes. Stirring was continued for 45 minutes, the resulting red solution was filtered and the filtrate was evaporated in vacuo to give a red solid. This red solid was dissolved in 30 ml of dioxan and added portionwise to a stirred solution of 1.25 g (0.013 mol) of penta-2,4-dienoic acid in 20 ml of dioxan. The red colour was allowed to fade between the additions. After completion of the addition and when no red colour persisted, the solution was stirred at room temperature for 1 hour and evaporated in vacuo to give a colourless solid. This solid was recrystallized from acetonitrile to give 1.17 g (43%) of 5-carboxy-2,3,5,8-tetrahydro-1,3-dioxo-1H-1,2,4-triazolo-[1,2-a]pyridazine-2-acetic acid of melting point 209°-211° C. (decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04307094
Source datasetuspto-grants-1981_12
ORD IDord-c0791d19e08644f8b588e256830e92c1
Source noteuspto-grants-1981_12