HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → HCID 20547117, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Methyl Ethyl Ketone | HCID 6569 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 20547116 | HCID 20547116 | — |
| Product | HCID 20547117 | HCID 20547117 | — |
Reaction Steps
A mixture of 19.9 g (0.05 mole) of 1,3-bis-(2,2,6,6-tetramethylpiperid-4-yl)-2-methyl-2-oxo-1,3,2-diazaphospholane (compound 1), 16.6 g of potassium carbonate, 0.3 g of finely powdered potassium iodide, 24.2 g of allyl bromide and 80 ml of ethyl methyl ketone is stirred for 18 hours at reflux temperature. The mixture is then filtered, the filtrate is freed from the solvent in vacuo and the residual crystalline crude product is recrystallised from acetonitrile, yielding pure 1,3-bis(1-allyl-2,2,6,6-tetramethylpiperid-4-yl)-2-methyl-2-oxo-1,3,2-diazaphospholane (compound 13) with a melting point of 168°-169° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04322531 |
| Source dataset | uspto-grants-1982_03 |
| ORD ID | ord-cb32de83a8af475a97e1c872b5aee2a0 |
| Source note | uspto-grants-1982_03 |