HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821437Generated: November 2, 2026
Water → [2-(4-Formyl-2-methoxy-3-nitrophenoxy)ethyl]propane-1-sulfonamide
https://huagongshe.com/reaction/1821437
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Propanesulfonyl chloride | HCID 66279 | — |
| Reactant | 2-(4-Dimethoxymethyl-2-methoxy-3-nitrophenoxy)ethylamine | HCID 68999463 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [2-(4-Formyl-2-methoxy-3-nitrophenoxy)ethyl]propane-1-sulfonamide | HCID 86628224 | 62.6% |
Reaction Steps
A solution of 2-(4-dimethoxymethyl-2-methoxy-3-nitrophenoxy)ethylamine (0.5 g, 1.8 mmol) obtained in Step 3 in THF (10 mL) was added with triethylamine (0.38 mL, 2.7 mmol) and n-propanesulfonyl chloride (0.24 mL, 2.2 mmol), followed by stirring at room temperature for 3 hours. The reaction mixture was added with water and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and the solvent was evaporated under reduced pressure. The residue was added with methanol (6.0 mL) and 1 mol/L hydrochloric acid, followed by stirring for 15 minutes. The reaction mixture was added with water and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and the solvent was evaporated under reduced pressure to obtain [2-(4-formyl-2-methoxy-3-nitrophenoxy)ethyl]propane-1-sulfonamide (0.39 g, 62%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07605272B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-aada1a53d84d4e73a5821c2af168b354 |
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| Source note | uspto-grants-2009_10 |
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