HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276080Generated: October 27, 2026
Sodium Iodide → N-1-butanesulfonyl-3-(2,4-dichlorobenzylamino)-4-nitrobenzamide
https://huagongshe.com/reaction/276080
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 2,4-Dichlorobenzyl chloride | HCID 7212 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-1-butanesulfonyl-3-amino-4-nitrobenzamide | HCID 18315533 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-1-butanesulfonyl-3-(2,4-dichlorobenzylamino)-4-nitrobenzamide | HCID 18315434 | 52.7% |
Reaction Steps
A solution containing 1.10 g of N-1-butanesulfonyl-3-amino-4-nitrobenzamide, 0.273 g of sodium iodide, 1.54 g of potassium carbonate, 2.17 g of 2,4-dichlorobenzyl chloride and 10 ml of methanol was stirred at 60° C. for 24 hours. Further, 2.00 g of 2,4-dichlorobenzyl chloride were added thereto, and the mixture was heated at 60° C. for 36 hours. To the reaction solution were added ethyl acetate and a saturated aqueous solution of sodium hydrogencarbonate, and N-1-butanesulfonyl-3-(2,4-dichlorobenzylamino)-4-nitrobenzamide was extracted in the aqueous layer. The organic layer was concentrated to give 0.885 g of N-1-butanesulfonyl-3-(2,4-dichlorobenzylamino)-4-nitrobenzamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06352985B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-898d436535db481595ac9e4346de175f |
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| Source note | uspto-grants-2002_03 |
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