Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757946Generated: November 2, 2026

Thionyl Chloride → HCID 13712584, compound

https://huagongshe.com/reaction/1757946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 13712582HCID 13712582—
ProductHCID 13712584HCID 1371258453%

Reaction Conditions

Temperature0 °C

Reaction Steps

0.5 g. (2 mmoles) of 2-acetyl-3-phenyl-4-hydroxymethyltetrahydro-1,2,4-oxadiazin-5-one are refluxed in 3 ml. of thionyl chloride for one hour. The solution is evaporated to dryness under reduced pressure. The residue is triturated with diethyl ether cooled to 0° C. and the product is filtered off and is subsequently recrystallized from a mixture of 2 ml. of chloroform and 6 ml. of n-hexane. 0.28 g. (53%) of 2-acetyl-3-phenyl-4-chloromethyl-tetrahydro-1,2,4-oxadiazin-5-one are obtained, melting at 171° to 172° C.; RfA =0.7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04371534
Source datasetuspto-grants-1983_02
ORD IDord-6d4e0fbb561e494cb0ab98bd3656b7ee
Source noteuspto-grants-1983_02