HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361429Generated: October 30, 2026
Diethanolamine → N,N-Bis-(2-hydroxy-ethyl)-2-nitrobenzenesulfonamide
https://huagongshe.com/reaction/1361429
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethanolamine | HCID 8113 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Nitrobenzenesulfonyl chloride | HCID 15540 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N,N-Bis-(2-hydroxy-ethyl)-2-nitrobenzenesulfonamide | HCID 60723400 | — |
Reaction Steps
A solution of 2-nitrobenzenesulfonyl chloride (10.5 g, 47.6 mmol) in anhydrous methylene chloride (25 mL) was added dropwise with stirring to a 0° C. solution of diethanolamine (5.00 g, 47.6 mmol) and triethylamine (4.92 g, 47.6 mmol) in anhydrous methylene chloride (50 mL). Reaction stirred three hours at 0° C. and then overnight at room temperature. Reaction mixture concentrated under reduced pressure. Residue dissolved in ethyl acetate, washed with 1 N NaOH, saturated NaHCO3, and brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. The residue was purified by normal phase HPLC on a Biotage pre-packed silica gel column eluting with ethyl acetate to afford the title compound. MS(ESI) m/z 291 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07880001B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-301e39da6e614b9b9a4334aa92c782ee |
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| Source note | uspto-grants-2011_02 |
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