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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468834Generated: November 2, 2026

Methyl iodide → 2-chloro-5-(MethoxyMethyl)pyriMidine

https://huagongshe.com/reaction/1468834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant(2-Chloropyrimidin-5-yl)methanolHCID 54150633—
SolventDimethylformamideHCID 6228—
Product2-chloro-5-(MethoxyMethyl)pyriMidineHCID 8671778566.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-chloro-5-hydroxymethyl-pyrimidine (9.0 g, 62 mmol) in 70 ml of anhydrous DMF was added methyl iodide (6 eq. 370 mmol, 23 ml). The mixture was cooled to 0° C., then NaH (2.61 g, 1.05 eq.) was added in portions over 5 mins. The resulting mixture was stirred 25 min. at 0° C., then 25 min. at rt. The reaction mixture was then cooled in ice bath, and quenched by addition of saturated NH4Cl aq. solution (200 ml), extracted with ether (150 ml×3). The combined organic layers were washed by brine, dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified by ISCO column (330 g of silica gel) using ethyl acetate in hexane (0-90% ethyl acetate, 2500 ml, then 1000 ml of ethyl acetate) to give 6.5 g (66%) of the title compound: MS (ESI) m/z 159.2 (M+H); 1H NMR (500 MHz, CDCl3) δ 8.60 (s, 2H), 4.48 (s, 2H), 3.45 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006228B2
Source datasetuspto-grants-2015_04
ORD IDord-4b3d421de4db46458b7d035cd9208ada
Source noteuspto-grants-2015_04