HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 2-(Iodomethyl)thio-5-chloropyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 2-Chloromethylthio-5-chloropyrimidine | HCID 13435135 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-(Iodomethyl)thio-5-chloropyrimidine | HCID 13435136 | 86% |
Reaction Steps
Sodium iodide (30 mmol) was added to a solution of 2-chloromethylthio-5-chloropyrimidine (6.7 mmol) in acetone (30 ml) and the mixture heated under reflux for 4 h. The precipitated sodium chloride was removed by filtration, the filtrate evaporated to dryness, the residue triturated with water and recrystallized from ethanol; yield 86%, m.p. 67° C. 1H NMR (CDCl3): δ4.82 (SCH2), 8.67 (H-4, H-6).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04423047 |
| Source dataset | uspto-grants-1983_12 |
| ORD ID | ord-12f0f7dc480e4c4da921b92593113ada |
| Source note | uspto-grants-1983_12 |