HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → HCID 66701620, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Chloro-2-fluoroaniline | HCID 75015 | — |
| Reactant | 2-Chloromethyl-8-(2-chloro-5-thiazolyl)methyl-1,4-dioxa-8-azaspiro[4,5]decane | HCID 66701610 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 66701620 | HCID 66701620 | 85% |
Reaction Steps
21 gm (0.065 mole) of 2-chloromethyl-8-(2-chloro-5-thiazolyl)methyl-1,4-dioxa-8-azaspiro[4,5]decane was taken in DMF (300 ml) at 28° C. To this mixture was added 28 gm of potassium carbonate, 10 gm of 5-chloro-2-fluoroaniline and the catalyst potassium iodide. The mass was kept at 140° C. for 20 hrs. The mixture was poured into ice-cooled water and the mass was extracted with ethyl acetate. The solvent was distilled off to get the dark brick red colored product with yield 85%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08841296B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-5a67262532a341e8b1f063b8e97b2994 |
| Source note | uspto-grants-2014_09 |