HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193436Generated: November 1, 2026
Ethyl chloroformate → 3-(2-Nitrophenyl)-1,2,4-oxadiazol-5(2H)-one
https://huagongshe.com/reaction/1193436
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Nitrobenzamidoxime | HCID 54293867 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 3-(2-Nitrophenyl)-1,2,4-oxadiazol-5(2H)-one | HCID 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., Yakugaku 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04810282 |
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| Source dataset | uspto-grants-1989_03 |
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| ORD ID | ord-15db57b04ea94ea5b0a34a6fa2e6d6d4 |
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| Source note | uspto-grants-1989_03 |
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