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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007245Generated: October 28, 2026

Methyl iodide → HCID 69879819, compound

https://huagongshe.com/reaction/1007245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 22668807HCID 22668807—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69879819HCID 6987981982.3%

Reaction Steps

To a solution of 2.5 g (6.8 mmol) of methyl 2-(difluoromethyl)-5-isothiocyanato-4-(2-methylpropyl)-6-(trifluoromethyl)-3-pyridinecarboxylate (U.S. Pat. No. 5,129,943 example 41 step A) in 25 ml of anhydrous THF at room temperature was added 1.6 g (7.5 mmol) of 25% sodium methoxide in methanol. The reaction mixture was stirred for 30 min and was treated with 1.93 g (14 mmol) of methyl iodide. The reaction mixture was stirred for 3 h and concentrated in vacuo. The residue was partitioned with ether (75 ml) and 10% HCl (50 ml). The organic layer was washed with water (3×30 ml), dried (MgSO4), and concentrated in vacuo. The crude product was purified by chromatotron (20% EtOAc in hexane) to afford 2.32 g (82%) of a colorless oil, n25D 1.5982.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06794396B2
Source datasetuspto-grants-2004_09
ORD IDord-1092a07d26c048809610333a13624827
Source noteuspto-grants-2004_09