HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3-[Cyclopropyl(4-ethoxy-4-oxobutyl)sulfamoyl]benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | 2-(Trimethylsilyl)ethyl 3-[cyclopropyl(4-ethoxy-4-oxobutyl)sulfamoyl]benzoate | HCID 71238737 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-[Cyclopropyl(4-ethoxy-4-oxobutyl)sulfamoyl]benzoic acid | HCID 71238622 | 96.7% |
Reaction Steps
A mixture of 2.48 g of 2-(trimethylsilyl)ethyl 3-[cyclopropyl(4-ethoxy-4-oxobutyl)sulfamoyl]benzoate, a solution of TBAF in THF (1.0 M, 10 mL), and 25 mL of THF was stirred at room temperature for 2 hours. To the reaction mixture was added 0.2 M hydrochloric acid, followed by extraction with ethyl acetate. The organic layer was washed with 0.2 M hydrochloric acid, water, saturated brine in this order, then dried over anhydrous sodium sulfate, and concentrated under reduced pressure to obtain 1.87 g of 3-[cyclopropyl(4-ethoxy-4-oxobutyl)sulfamoyl]benzoic acid as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08729068B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-2dca3966b03f4414911d85a329e67907 |
| Source note | uspto-grants-2014_05 |