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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820724Generated: November 1, 2026

Methyl iodide → 5-Methanesulfonyl-2-trifluoromethoxy-benzoic acid

https://huagongshe.com/reaction/1820724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantBenzoic acid, 5-sulfino-2-(trifluoromethoxy)-HCID 69037717—
SolventDimethylformamideHCID 6228—
Product5-Methanesulfonyl-2-trifluoromethoxy-benzoic acidHCID 69039047—

Reaction Steps

To 5-Sulfino-2-trifluoromethoxy-benzoic acid (0.82 g) in DMF (5 mL) was added 1.3 g of potassium carbonate, and the reaction mixture was stirred for 5 minutes before methyl iodide (0.66 mL) was added. The reaction mixture was then stirred at room temperature for 60 hours. After such time the reaction mixture was concentrated in vacuo, and the residue was treated with 1N NaOH (10 mL) and THF (4 mL). The reaction mixture was stirred for a further 2 hours at room temperature. After such time the solution was acidified with concentrated HCl solution. THF was then removed in vacuo, and the precipitate was isolated by filtration and washed several times with water to yield the title compound. MS (m/e): 283.0 (M−H, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07605163B2
Source datasetuspto-grants-2009_10
ORD IDord-2ab9849ee1944bb397993fe1b539e700
Source noteuspto-grants-2009_10