HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075434Generated: October 30, 2026
Hydrochloric Acid → 4-Dimethoxymethyl-1-(2-morpholinoethoxy)-2-nitrobenzene
https://huagongshe.com/reaction/2075434
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(2-Morpholinoethoxy)-3-nitrobenzaldehyde hydrochloride | HCID 23117920 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Dimethoxymethyl-1-(2-morpholinoethoxy)-2-nitrobenzene | HCID 23117902 | 97.4% |
Reaction Steps
A solution of 4-(2-morpholinoethoxy)-3-nitrobenzaldehyde hydrochloride obtained in Step 1 (2.97 g, 9.38 mmol) in dichloromethane (10.0 mL) was added with trimethyl orthoformate (15.0 mL, 13.7 mmol) and a 10% solution of hydrogen chloride in methanol (5.00 mL), followed by stirring at room temperature for 4 hours. The reaction mixture was added with potassium carbonate (10.0 g, 72.4 mmol), then stirred at room temperature for 5 hours, and the solvent was evaporated under reduced pressure. The residue was added with water (50 mL) and was extracted with ethyl acetate (50 mL×3). After drying over anhydrous sodium sulfate, the solvent was evaporated under reduced pressure to obtain 4-dimethoxymethyl-1-(2-morpholinoethoxy)-2-nitrobenzene (2.98 g, 97%).
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-7a26484fe7ab416a8aaea2f238edf426 |
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| Source note | uspto-grants-2011_04 |
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