HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177263Generated: October 30, 2026
Water → Ethyl 2-ethyl-4-[4-(methylsulfonyl)phenoxy]-1-benzofuran-6-carboxylate
https://huagongshe.com/reaction/1177263
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1-Fluoro-4-(methylsulphonyl)benzene | HCID 67994 | — |
| Reactant | Ethyl 2-ethyl-4-hydroxy-1-benzofuran-6-carboxylate | HCID 59560005 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 2-ethyl-4-[4-(methylsulfonyl)phenoxy]-1-benzofuran-6-carboxylate | HCID 59560127 | 60.6% |
Reaction Steps
A mixture of ethyl 2-ethyl-4-hydroxy-1-benzofuran-6-carboxylate (0.80 g, 3.4 mmol), 4-fluorophenyl methyl sulfone (0.60 g, 3.4 mmol) and Cs2CO3 (1.12 g, 3.4 mmol) in DMF (40 mL) was heated to 100° C. overnight. The reaction was monitored by TLC (petroleum ether/EtOAc 4:1). The mixture was poured into water (50 mL) and extracted with EtOAc (90 mL×3). The organic layer was washed with brine (50 mL×2), dried over Na2SO4 and concentrated. The product was purified via column chromatography on silica gel eluted with petroleum ether/EtOAc (20:1) to afford the desired compound (0.80 g, 60%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07842713B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-04983dd0f8534b99a18a1d2cbba7971c |
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| Source note | uspto-grants-2010_11 |
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