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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Bromoethyl methyl ether | HCID 80972 | — |
| Reactant | Methyl 3-hydroxy-4-methanesulfonyl-2-methylbenzoate | HCID 18694846 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 3-(2-methoxyethoxy)-2-methyl-4-(methylsulfonyl)benzoate | HCID 66755969 | 55% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08466088B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-52275aa1c91f463598b9979008afc27c |
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| Source note | uspto-grants-2013_06 |
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