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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241740Generated: October 27, 2026

Sodium hydride → 5-(4-Chlorophenyl)-3,6-dihydro-2H-1,3,4-oxadiazin-2-one

https://huagongshe.com/reaction/241740

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantEthyl N'-[1-(4-chloro-phenyl)-2-hydroxy-ethylidene]-hydrazinecarboxylateHCID 86662431—
SolventEthanolHCID 702—
Product5-(4-Chlorophenyl)-3,6-dihydro-2H-1,3,4-oxadiazin-2-oneHCID 13365915—

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium hydride (60% in oil, 16 mmoles) is added, in small portions and at ambient temperature, to a solution of the compound obtained in Step B (100.5 mmoles) in ethanol (800 ml). After reacting for 2 hours, the reaction mixture is cooled to 0° C. and stiffing is continued for 30 minutes. The precipitate formed is filtered off, washed with cold ethanol and then dried in vacuo to yield the title product, which is used directly in the next Step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653073B2
Source datasetuspto-grants-2014_02
ORD IDord-2b7b449cd0a94fb88bc5f0d70a3b0284
Source noteuspto-grants-2014_02