HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213859Generated: October 31, 2026
Nitric Acid → Ethyl 3-methoxy-4-(3-morpholinopropoxy)-6-nitrobenzoate
https://huagongshe.com/reaction/2213859
Participants
| Role | Name | HCID | Charge |
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| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | HCID 21958890 | HCID 21958890 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 3-methoxy-4-(3-morpholinopropoxy)-6-nitrobenzoate | HCID 11773033 | 161.8% |
Reaction Steps
Concentrated sulphuric acid (110 ml) and concentrated nitric acid (19.0 ml, 0.289 mol) were added cautiously, over a 50 minute period, to a two-phase system containing a stirred solution of ethyl 3-methoxy-4-(3-morpholinopropoxy)benzoate (76.5 g, 0.237 mol) in dichloromethane (600 ml), acetic acid (300 ml) and water (70 ml) at 5° C. The reaction was allowed to warm to ambient temperature over 18 hours, the aqueous phase was separated, and the aqueous phase was taken to pH 9 by addition of 40% aqueous sodium hydroxide solution (775 ml). Extraction of the aqueous phase with dichloromethane (3×600 ml) and subsequent solvent evaporation in vacuo yielded ethyl 3-methoxy-4-(3-morpholinopropoxy)-6-nitrobenzoate (141.3 g, 86% yield) as a yellow gum:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07105669B1 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-b9c40cfb6f7b4982b314a98000b39a72 |
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| Source note | uspto-grants-2006_09 |
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