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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 364834Generated: November 1, 2026

Ethyl chloroformate → 3-(2-Nitrophenyl)-1,2,4-oxadiazol-5(2H)-one

https://huagongshe.com/reaction/364834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantNitrobenzamidoximeHCID 54293867—
SolventPyridineHCID 1049—
Product3-(2-Nitrophenyl)-1,2,4-oxadiazol-5(2H)-oneHCID 136040260—

Reaction Steps

The reactions of Equation 41 above can be run by methods known in the art. Thus, in reaction 41a, 2-nitrobenzamidoxime LII is reacted with ethyl chloroformate in excess pyridine at 0° to 100° C. for about 1 hour to form a 3-(2-nitrophenyl)-1,2,4-oxadiazolin-5-one of Formula (LIV), according to the teachings of A. R. Katritzky et al., Tetrahedron, 21, 1681 (1965). In reaction 41b, LIV is reacted with excess phosphorus oxychloride or phosphorus oxybromide with pyridine catalyst at 25° to 100° C. for 1 to 15 hours to form X1"', according to the teachings of T. Fujita et al., Yakagaku Zasshi, 84, 1061 (1964). And in reaction 41c, X1"' is reacted with sodium methoxide or sodium ethoxide in a solvent such as methanol, ethanol or tetrahydrofuran at 20° to 50° C. for about 0.2 to 1 hour to form X1"", according to the teachings of F. Eloy et al., Bull. Soc. Chim. Belg., 78, 47 (1969).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04606755
Source datasetuspto-grants-1986_08
ORD IDord-a00b8546753747cc99ef06a97fcf349d
Source noteuspto-grants-1986_08