HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1268123Generated: October 27, 2026
Acetic Anhydride → N-[2-[3-(4-t-Butylbenzyloxy)benzamido]benzenesulfonyl]acetamide
https://huagongshe.com/reaction/1268123
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 3-(4-t-Butylbenzyloxy)-N-(2-sulfamoylphenyl)benzamide | HCID 12041309 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[2-[3-(4-t-Butylbenzyloxy)benzamido]benzenesulfonyl]acetamide | HCID 18544150 | 96% |
Reaction Steps
In a stream of nitrogen and at 0° C., 0.11 ml (1.10 mmol) of acetic anhydride was added to an anhydrous tetrahydrofuran (10 ml) solution containing 438 mg (1.00 mmol) of 3-(4-t-butylbenzyloxy)-N-(2-sulfamoylphenyl)benzamide produced in Reference Example 2 and 249 mg (2.00 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 456 mg (yield: 96.0%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06555584B1 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-a72975e3f8ed40448f0876351dd64398 |
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| Source note | uspto-grants-2003_04 |
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