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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757943Generated: November 3, 2026

Acetic Anhydride → HCID 13712581, compound

https://huagongshe.com/reaction/1757943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 20510399HCID 20510399—
CatalystPalladiumHCID 23938—
ProductHCID 13712581HCID 1371258182%

Reaction Steps

0.69 g. (2 mmoles) of 2-benzyloxycarbonyl-3-phenyl-4-ethyl-tetrahydro-1,2,4-oxadiazin-5-one are dissolved in 7 ml. of acetic anhydride, 0.1 g. of a 5%, palladium-on-activated carbon catalyst are added and hydrogen gas is bubbled through the mixture at room temperature under vigorous stirring. The progress of hydrogenation is monitored by thin layer chromatography. As soon as the reaction is complete, the catalyst is filtered off, the filtrate is evaporated to dryness under reduced pressure and the residue is recrystallized from 1 ml. of ethanol. 0.41 g. (82%) of 2-acetyl-3-phenyl-4-ethyl-tetrahydro-1,2,4-oxadiazin-5-one are obtained, melting at 130° C. to 132° C. RfA =0.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04371534
Source datasetuspto-grants-1983_02
ORD IDord-f2f0afe947c54fb5abe987c32197b40b
Source noteuspto-grants-1983_02