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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257995Generated: November 1, 2026

Potassium Iodide → Methyl 3-(2-methoxyethoxy)-2-methyl-4-(methylsulfonyl)benzoate

https://huagongshe.com/reaction/1257995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium hydrideHCID 24758—
Reactant2-Bromoethyl methyl etherHCID 80972—
ReactantMethyl 3-hydroxy-4-methanesulfonyl-2-methylbenzoateHCID 18694846—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductMethyl 3-(2-methoxyethoxy)-2-methyl-4-(methylsulfonyl)benzoateHCID 6675596955%

Reaction Steps

To a stirred suspension of sodium hydride (60%, 220 mg, 5.32 mmol) in anhydrous N,N-dimethylformamide (10 mL) was added methyl 3-hydroxy-2-methyl-4-(methylsulfonyl)benzoate (1 g, 4.09 mmol) under nitrogen atmosphere at room temperature. After stirring for 30 minutes, 2-bromoethyl methyl ether (1.13 g, 8.18 mmol) and potassium iodide in a catalytic amount were added thereto, and the reaction solution was stirred at 60° C. for 12 hours. 200 mL of ethyl acetate was added to the reaction solution, and the solution was washed twice with a saturate brine. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=1:2) to obtain methyl 3-(2-methoxyethoxy)-2-methyl-4-(methylsulfonyl)benzoate as an oil (680 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466088B2
Source datasetuspto-grants-2013_06
ORD IDord-52275aa1c91f463598b9979008afc27c
Source noteuspto-grants-2013_06