HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Iodosuccinimide → 6-Ethyl-5-iodopyrimidin-4(1H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | HCID 178436949 | HCID 178436949 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 6-Ethyl-5-iodopyrimidin-4(1H)-one | HCID 135706148 | — |
Reaction Steps
To a stirred solution of 70 g (0.56 mol) 4-hydroxy-6-ethyl pyrimidine in acetic acid is added 127 g (0.56 mol) NIS portion wise at RT within 15 min. The reaction is stirred for 30 h at RT until all starting material is consumed. The reaction mixture is diluted with water and the solid product is filtered off and washed with sodium thiosulfate solution to remove excess iodine. After drying, the desired product is obtained as a solid (90 g; 64%) which is used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09321771B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-0ea8e1885d15413e877da5d126ea57b4 |
| Source note | uspto-grants-2016_04 |