HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11761Generated: October 25, 2026
Sodium Iodide → 2,4-Dichloro-5-(iodomethyl)pyrimidine
https://huagongshe.com/reaction/11761
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 2,4-Dichloro-5-(chloromethyl)pyrimidine | HCID 13568279 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2,4-Dichloro-5-(iodomethyl)pyrimidine | HCID 21939352 | — |
Reaction Steps
A 500-mL, round-bottom flask equipped with a magnetic stirrer, condenser, and nitrogen-inlet bubbler was charged with sodium iodide (38.5 g, 256.9 mmol) (Aldrich) and acetone (300 mL). After a clear solution was obtained, 2,4-dichloro-5-(chloromethyl)pyrimidine (50.0 g, 253.2 mmol) (from Example 1b supra) was added in one portion. After stirring at room temperature for 20 minutes, the mixture was heated to reflux for 15 minutes. NMR analysis indicated 98% conversion. After cooling to room temperature, the resulting precipitate (sodium chloride) was removed by filtration through a medium-sintered glass funnel and washed with acetone. The combined filtrate and washes were concentrated to a weight of ca. 75 g. The resulting concentrated solution of 2,4-dichloro-5-(iodomethyl)pyrimidine in acetone was diluted with toluene (20 mL). After concentration to a weight of ca.85 g in order to remove the residual acetone, this concentrated solution of 2,4-dichloro-5-(iodomethyl)pyrimidine in toluene was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07098332B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-c65460f7404d4c359602cdb11f0d47b8 |
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| Source note | uspto-grants-2006_08 |
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