HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926037Generated: October 26, 2026
Dimethylformamide → 2-(Trimethylsilyl)ethyl 3-[cyclopropyl(4-ethoxy-4-oxobutyl)sulfamoyl]benzoate
https://huagongshe.com/reaction/926037
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 4-bromobutyrate | HCID 76300 | — |
| Reactant | 2-(Trimethylsilyl)ethyl 3-(cyclopropylsulfamoyl)benzoate | HCID 71238446 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(Trimethylsilyl)ethyl 3-[cyclopropyl(4-ethoxy-4-oxobutyl)sulfamoyl]benzoate | HCID 71238737 | 87.7% |
Reaction Steps
A mixture of 2.12 g of 2-(trimethylsilyl)ethyl 3-(cyclopropylsulfamoyl)benzoate, 1.45 g of ethyl 4-bromobutyrate, 2.57 g of potassium carbonate, and 21 mL of DMF was stirred at 80° C. overnight. To the reaction mixture was added water, followed by extraction with ethyl acetate. The organic layer was washed with water and saturated brine in this order, then dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane-ethyl acetate) to obtain 2.48 g of 2-(trimethylsilyl)ethyl 3-[cyclopropyl(4-ethoxy-4-oxobutyl)sulfamoyl]benzoate as a colorless oily substance. ESI+: 456
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09284295B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-bfbae0cf377c43cda65cebf021422f12 |
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| Source note | uspto-grants-2016_03 |
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