HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1268111Generated: October 26, 2026
Decanoyl chloride → N-[2-[3-(4-Chlorobenzyloxy)benzamido]benzenesulfonyl]decanamide
https://huagongshe.com/reaction/1268111
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Decanoyl chloride | HCID 66982 | — |
| Reactant | 3-(4-Chlorobenzyloxy)-N-(2-sulfamoylphenyl)benzamide | HCID 12041315 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[2-[3-(4-Chlorobenzyloxy)benzamido]benzenesulfonyl]decanamide | HCID 12041316 | 93.4% |
Reaction Steps
In a stream of nitrogen and at 0° C., 0.27 ml (1.30 mmol) of decanoyl chloride was added to an anhydrous tetrahydrofuran (10 ml) solution containing 500 mg (1.20 mmol) of 3-(4-chlorobenzyloxy)-N-(2-sulfamoylphenyl)benzamide produced in Reference Example 4 and 293 mg (2.40 mmol) of 4-dimethylaminopyridine, the mixture was stirred at room temperature for 1 hour and then the solvent was evaporated under a reduced pressure. The resulting residue was dissolved in ethyl acetate, washed with water, a potassium hydrgensulfate aqueous solution and saturated brine in that order and dried over anhydrous sodium sulfate, and then the solvent was evaporated under a reduced pressure. The resulting residue was purified by a silica gel column chromatography to obtain 640 mg (yield: 93.0%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06555584B1 |
|---|
| Source dataset | uspto-grants-2003_04 |
|---|
| ORD ID | ord-db9fc67fd2704242bcd9259842a96324 |
|---|
| Source note | uspto-grants-2003_04 |
|---|