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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2400120Generated: November 4, 2026

Methyl iodide → HCID 67715083, compound

https://huagongshe.com/reaction/2400120

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantMethyl formateHCID 7865—
ReactantSodium hydrideHCID 24758—
ReactantHCID 19044668HCID 19044668—
SolventDiethyl EtherHCID 3283—
ProductHCID 67715083HCID 67715083—

Reaction Steps

Ethyl α-[2-methyl-4-(3-trifluoromethylphenoxy)-5-pyrimidinyl]-acetate (3 g, 8 mmol) are dissolved in methyl formate (10 ml) and added to a suspension of NaH (0.6 g, 80% in oil, 20 mmol) in 1,2-dimethoxyaethane at room temperature. After 16 hours methyl iodide (2.5 ml, 40 mmol) is added with cooling. After further 2 hours the reaction mixture is diluted with ether and washed with brine. Drying and chromatography on silicagel (eluant: hexane/ethyl acetate 1:1) gives the methyl α-[2-methyl-4-(3-trifluoromethylphenoxy)-5-pyrimidinyl]-β-methoxyacrylate compound as a crystalline solid, m.p. 100°-102° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05453427
Source datasetuspto-grants-1995_09
ORD IDord-62f9a0e81d1842ffa5bfb12a56788b5c
Source noteuspto-grants-1995_09