HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713498Generated: October 25, 2026
Triethylamine → N-cyclopropyl-2-nitrobenzenesulfonamide
https://huagongshe.com/reaction/1713498
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Nitrobenzenesulfonyl chloride | HCID 15540 | — |
| Reactant | Cyclopropylamine | HCID 69828 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-cyclopropyl-2-nitrobenzenesulfonamide | HCID 796630 | 87% |
Reaction Steps
To a solution of cyclopropylamine (1.0 g, 18 mmol) and triethylamine (3.7 mL, 27 mmol) in tetrahydrofuran (20 mL) was added 2-nitrobenzenesulfonyl chloride (3.9 g, 18 mmol) at 0° C., and the mixture was stirred at 0° C. for 1 hour. The solvent was distilled off under reduced pressure, and the residue was diluted with ethyl acetate. The reaction solution was washed with water and saturated brine and dried over magnesium sulfate. The solid was filtered off, and the filtrate was concentrated. The residue was purified with silica gel column chromatography (hexane:ethyl acetate=1:1) and concentrated. The residue was washed with hexane and collected by filtration to obtain the title compound (3.7 g, 87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07795267B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-54aa42dedd6945a3ae83e85f9e326f61 |
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| Source note | uspto-grants-2010_09 |
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