Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1763513Generated: October 28, 2026

Propargyl alcohol → Pirquinozol

https://huagongshe.com/reaction/1763513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl alcoholHCID 7859—
Reactant(3Z)-3-diazo-1H-indol-2-oneHCID 136455454—
SolventBenzeneHCID 241—
ProductPirquinozolHCID 13544934023%

Reaction Steps

4.8 g (0.03 mole) of 3-diazooxindole is suspended in 500 ml of benzene and 1.96 g (0.033 mole) of propargyl alcohol added. The reaction mixture is refluxed overnight under nitrogen, after which 19.6 g (0.33 mole) of propargyl alcohol is added and the reaction continued under reflux for a total of 48 hours. The tan solid which precipitates is filtered off (1.5 g, 23% yield), m.p. 272°-275° (sl. dec.). Recrystallization from methanol gives crystals of the title compound, m.p. 286°-288° (sl. dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04112096
Source datasetuspto-grants-1978_09
ORD IDord-012b95cbe7ca4d869a42f0e1cd600123
Source noteuspto-grants-1978_09