Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyanuric fluoride | HCID 12664 | — |
| Reactant | HCID 118413340 | HCID 118413340 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 90111611 | HCID 90111611 | — |
Reaction Steps
To a cold (0° C.) solution of 1,3-dimethyl-2-imidazolidinone oxime (prepared according Kitamura, Mitsuru; Chiba, Shunsuke; Narasaka, Koichi, Bulletin of the Chemical Society of Japan (2003), 76(5), 1063-1070) (5.3 g, 0.041 mol) in dry pyridine (25 ml) within 15 minutes is dropwise added cyanuric fluoride (1.49 g, 0.011 mol). The mixture is then heated for 2 h at 42° C. and then stirred for 15 h at room temperature. The pyridine is evaporated under reduced pressure, the residue is chromatographed (silica gel, CH2Cl2—CH3OH 20:1 to 10:1) and the pure fractions are crystallized from ethyl acetate hexane to afford 2.4 g of the title compound as white crystalls, mp. 143-145° C. (decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09255217B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-5f433eded7224ae79cb70c78bb0431bc |
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| Source note | uspto-grants-2016_02 |
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