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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094008Generated: October 27, 2026

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

https://huagongshe.com/reaction/1094008

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 stirring 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 numberUS08133889B2
Source datasetuspto-grants-2012_03
ORD IDord-26a52b66514f4965b5fb8672e9f7b39a
Source noteuspto-grants-2012_03