HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52001Generated: October 27, 2026
Potassium Carbonate → Benzyl 5-(4,6-Dimethoxy-1,3,5-triazin-2-yl)oxy-2-methyl-3-methoxycarbonylbenzofuran-4-carboxylate
https://huagongshe.com/reaction/52001
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4,6-Dimethoxy-2-methylsulfonyl-1,3,5-triazine | HCID 15790044 | — |
| Reactant | Benzyl 5-hydroxy-2-methyl-3-methoxycarbonylbenzofuran-4-carboxylate | HCID 54269833 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Benzyl 5-(4,6-Dimethoxy-1,3,5-triazin-2-yl)oxy-2-methyl-3-methoxycarbonylbenzofuran-4-carboxylate | HCID 54466231 | 109.7% |
Reaction Steps
A mixture comprising 2 g of benzyl 5-hydroxy-2-methyl-3-methoxycarbonylbenzofuran-4-carboxylate, 1 g of 4,6-dimethoxy-2-methylsulfonyl-1,3,5-triazine and 1 g of potassium carbonate in 20 ml of N,N-dimethylformamide, was heated and stirred at 70° C. for two hours. The mixture was returned to room temperature, poured into ice water and extracted with ethyl acetate. The organic layer was washed with water and then dried over anhydrous sodium sulfate. Then, it was concentrated under reduced pressure, and the obtained solid was thoroughly washed with ethanol to obtain 2.4 g (yield: 86%) of the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05616537 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-c8aeca6db46d47d69486361733e264f1 |
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| Source note | uspto-grants-1997_04 |
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