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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660502Generated: November 2, 2026

Cyclohexylamine → HCID 178478536, compound

https://huagongshe.com/reaction/1660502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexylamineHCID 7965—
ReactantHCID 178478441HCID 178478441—
ProductHCID 178478536HCID 178478536—

Reaction Steps

To 5.0 g. of 3-phenyl-6-chloromethyl-5,6-dihydro-4H-1,2,4-oxadiazine (Chem. Ber. 108, 1911 (1975) 37 ml. of cyclohexyl amine are added. The reaction mixture is then refluxed for 10 hours. The excess of cyclohexyl amine is evaporated in vacuo and to the evaporation residue 100 ml. of ethyl acetate are added. The mixture is brought to the boil and the insoluble substances are filtered off while hot. The mother liquor is evaporated in vacuo, the residue is dissolved in isopropanol and the solution is acidified by introducing hydrogen chloride gas. 4.0 g. of 3-phenyl-6-cyclohexylaminomethyl-5,6-dihydro-4H-1,2,4-oxadiazine dihydrochloride are obtained, melting at 240° to 244° C. (after recrystallization from isopropanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04308270
Source datasetuspto-grants-1981_12
ORD IDord-b754945b0af94898865b3a4da717ff38
Source noteuspto-grants-1981_12