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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500137Generated: October 30, 2026

Methyl iodide → Methyl 2-fluoro-4-[3-(methylthio)-1,2,4-triazin-6-yl]benzoate

https://huagongshe.com/reaction/500137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantThiosemicarbazideHCID 2723789—
ReactantHCID 59216307HCID 59216307—
SolventEthanolHCID 702—
ProductMethyl 2-fluoro-4-[3-(methylthio)-1,2,4-triazin-6-yl]benzoateHCID 59216327—

Reaction Conditions

Temperature90 °C

Reaction Steps

Methyl 4-(diethoxyacetyl)-2-fluorobenzoate (3.0 g, 0.01 mol) was dissolved in ethanol (30 mL). Thiosemicarbazide (1.2 g, 0.013 mol) and p-toluenesulfonic acid monohydrate (100 mg) were added to the reaction mixture. The reaction mixture was heated at 90° C. for 2 h. After cooling, the reaction mixture to ambient temperature methyl iodide (3 mL, 0.05 mol) was added. The reaction mixture was stirred at RT for 2 h, and then concentrated under reduced pressure. The residue was dissolved in acetic acid (50 mL), and heated at 60° C. for 2 h. The reaction mixture was concentrated under reduced pressure. The residue was taken up in methanol and the precipitate was collected by filtration and dried under reduced pressure to give the desired product. (1.2 g, 41%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767675B2
Source datasetuspto-grants-2010_08
ORD IDord-833f8d89948b4956a4d1fdfb46cbff42
Source noteuspto-grants-2010_08