HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20491Generated: October 25, 2026
Potassium Carbonate → Methyl 3-(benzyloxy)-5-[4-(methanesulfonyl)phenoxy]benzoate
https://huagongshe.com/reaction/20491
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Fluoro-4-(methylsulphonyl)benzene | HCID 67994 | — |
| Reactant | Methyl 3-(benzyloxy)-5-hydroxybenzoate | HCID 7472028 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 3-(benzyloxy)-5-[4-(methanesulfonyl)phenoxy]benzoate | HCID 53393370 | 73.2% |
Reaction Steps
Potassium carbonate (3.21 g, 23.2 mmol) was added to a solution of methyl 3-hydroxy-5-{[phenylmethyl]oxy}benzoate (3.00 g, 11.6 mmol) in DMF (30 mL) followed by addition of 1-fluoro-4-(methylsulfonyl)benzene (2.02 g, 11.6 mmol) and the reaction was heated at 120° C. for 3 h. The solvent was then removed in vacuo and the residue was taken up in saturated aqueous sodium hydrogencarbonate (50 mL) and ethyl acetate (150 mL). The organic layer was separated, washed with 1M aqueous hydrochloric acid (50 mL) then dried (MgSO4), filtered and evaporated. Purification by column chromatography, eluting with 1:4 to 1:1 ethyl acetate:hexanes, afforded the title compound as a colourless oil (3.50 g, 73%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07745475B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-6af20b50dd1745cd86d2fc92c70fc7a5 |
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| Source note | uspto-grants-2010_06 |
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