HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816271Generated: November 1, 2026
Methylamine → N-methyl-2-nitrobenzene-1-sulfonamide
https://huagongshe.com/reaction/1816271
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 2-Nitrobenzenesulfonyl chloride | HCID 15540 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-methyl-2-nitrobenzene-1-sulfonamide | HCID 264906 | — |
Reaction Steps
To a solution of 2-nitrobenzenesulfonyl chloride (25 g, 0.113 mol) and dichloromethane (450 mL) at 4° C. was added dropwise 2M methylamine in tetrahydrofuran (68 mL). The mixture was stirred overnight allowing the ice bath to melt. More 2M methylamine in tetrahydrofuran (97 mL) was added and the reaction was stirred for 1 hour. The reaction mixture was concentrated in vacuo. The residue was dissolved in chloroform (500 mL) and was washed with saturated sodium bicarbonate (250 mL). The aqueous layer was extracted with chloroform (250 mL) and all the chloroform layers combined, dried over sodium sulfate and filtered. The filtrate was concentrated in vacuo and the residue purified by silica gel chromatography using 0-4% methanol in dichloromethane. 22.63 g of N-methyl-2-nitrobenzenesulfonamide was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06884801B1 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-4e6a4e89cb304485baec965320cb4319 |
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| Source note | uspto-grants-2005_04 |
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