HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1687428Generated: November 1, 2026
Dimethylformamide → 5-Dimethylamino-N,N-dimethyl-2-nitro-benzenesulfonamide
https://huagongshe.com/reaction/1687428
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Dimethylamine, hydrochloride | HCID 10473 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Chloro-N,N-dimethyl-2-nitro-benzenesulfonamide | HCID 67264233 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Dimethylamino-N,N-dimethyl-2-nitro-benzenesulfonamide | HCID 67263531 | — |
Reaction Steps
To a suspension of 5-Chloro-N,N-dimethyl-2-nitro-benzenesulfonamide (1.8 g, 0.0068 mol) and Potassium carbonate (3.3 g, 0.024 mol) in N,N-Dimethylformamide (20 mL, 0.2 mol) was added Dimethylamine hydrochloride (0.83 g, 0.010 mol). The suspension was heated at 50° C. The mixture was cooled to room temperature and poured into water. The precipitate was filtered and rinsed with water then hexane. The recovered material was purified by silica gel chromatography using 0%→20% Methanol:Dichloromethane solvent gradient. 5-Dimethylamino-N,N-dimethyl-2-nitro-benzenesulfonamide isolated as a yellow solid (0.55 g, 30%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08148391B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-183c181444e1408db5dbd4de7cd12ab0 |
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| Source note | uspto-grants-2012_04 |
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