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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant2,4-Dichloro-5-(chloromethyl)pyrimidineHCID 13568279—
SolventAcetoneHCID 180—
Product2,4-Dichloro-5-(iodomethyl)pyrimidineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07098332B2
Source datasetuspto-grants-2006_08
ORD IDord-c65460f7404d4c359602cdb11f0d47b8
Source noteuspto-grants-2006_08