HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexylamine → HCID 178478536, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexylamine | HCID 7965 | — |
| Reactant | HCID 178478441 | HCID 178478441 | — |
| Product | HCID 178478536 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04308270 |
| Source dataset | uspto-grants-1981_12 |
| ORD ID | ord-b754945b0af94898865b3a4da717ff38 |
| Source note | uspto-grants-1981_12 |