Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732763Generated: October 30, 2026

Methyl iodide → 2-Trifluoromethylthioanisole

https://huagongshe.com/reaction/732763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Trifluoromethyl)benzenethiolHCID 2777889—
SolventDimethylformamideHCID 6228—
Product2-TrifluoromethylthioanisoleHCID 276078388.3%

Reaction Steps

Dissolve 2-trifluoromethyl-benzenethiol (10 g, 56 mmol), potassium carbonate (25 g, 180 mmol), iodomethane (11 mL, 177 mmol) in DMF (100 mL). Stir for 12 hours. Filter the suspension through a pad of silica gel and elute with ethyl acetate (500 mL). Evaporate half of the solvent and wash the remaining solution with 10% aqueous LiCl (100 mL). Dry with MgSO4 and evaporate solvent. Chromatograph the residue on a SiO2 column eluting with hexane to give 9.5 g of 1-methylsulfanyl-2-trifluoromethyl-benzene (88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585977B2
Source datasetuspto-grants-2009_09
ORD IDord-1dcc37024a1b4713881d06f1f0f0ff72
Source noteuspto-grants-2009_09