HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495206Generated: October 29, 2026
Ethanolamine → N-(2-hydroxyethyl)-2-nitrobenzenesulfonamide
https://huagongshe.com/reaction/495206
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2-Nitrobenzenesulfonyl chloride | HCID 15540 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(2-hydroxyethyl)-2-nitrobenzenesulfonamide | HCID 3102011 | 78.1% |
Reaction Steps
2-Aminoethanol (4.0 mL, 66 mmol) was dissolved in N,N-dimethylformamide (50 mL). After the solution was cooled to −10° C., 2-nitrobenzenesulfonyl chloride (12 g, 52 mmol) and pyridine (4.7 mL, 58 mmol) were added dropwise thereto, followed by stirring for 50 minutes, while the temperature was raised to room temperature. To the reaction mixture was added water (0.20 L), and the mixture was extracted with ethyl acetate (0.10 L×6). The organic layer was dried over anhydrous sodium sulfate and then concentrated under reduced pressure to obtain N-(2-hydroxyethyl)-2-nitrobenzenesulfonamide (10 g, 62%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07538224B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-3d4f1846d8f24ece99e7654a17270136 |
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| Source note | uspto-grants-2009_05 |
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