HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075436Generated: October 31, 2026
Hydrochloric Acid → 3-Methanesulfonylamino-4-(2-morpholinoethoxy)benzaldehyde
https://huagongshe.com/reaction/2075436
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5-Dimethoxymethyl-2-(2-morpholinoethoxy)aniline | HCID 23117901 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Methanesulfonylamino-4-(2-morpholinoethoxy)benzaldehyde | HCID 23117895 | 95% |
Reaction Steps
A solution of 5-dimethoxymethyl-2-(2-morpholinoethoxy)aniline obtained in Step 3 (0.27 g, 0.91 mmol) in dichloromethane (2.00 mL) was added with methanesulfonyl chloride (0.11 mL, 1.42 mmol) and pyridine (0.50 mL, 6.18 mmol), followed by stirring at room temperature for 10 hours. The reaction mixture was added with hydrochloric acid (3 mol/L, 3.00 mL), was stirred at room temperature for 20 minutes, was neutralized with a saturated aqueous sodium hydrogencarbonate solution (50 ml) and was extracted with ethyl acetate (50 mL×3). The organic layer was dried over anhydrous sodium sulfate, the solvent was evaporated under reduced pressure. the crude product was purified by silica gel column chromatography (chloroform, then methanol/chloroform=1/6) to obtain 3-methanesulfonylamino-4-(2-morpholinoethoxy)benzaldehyde (0.28 g, 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07919517B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-10a1455f3c814ca6a634ba8e02987fd0 |
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| Source note | uspto-grants-2011_04 |
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