HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238972Generated: October 29, 2026
Nitric Acid → 1-[3-(2-Methoxy-5-nitro-phenyl)-pyrrolidin-1-yl]-propan-1-one
https://huagongshe.com/reaction/238972
Participants
| Role | Name | HCID | Charge |
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| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-[3-(2-Methoxy-phenyl)-pyrrolidin-1-yl]-propan-1-one | HCID 68954461 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Nitromethane | HCID 6375 | — |
| Product | 1-[3-(2-Methoxy-5-nitro-phenyl)-pyrrolidin-1-yl]-propan-1-one | HCID 68949938 | 101.8% |
Reaction Steps
1-[3-(2-Methoxy-phenyl)-pyrrolidin-1-yl]-propan-1-one (0.7 g; 3 mmol) were dissolved in 10 ml of nitromethane. At −5° C. to −10° C., a mixture of 0.290 g nitric acid, 0.5 g water and 5.52 g sulphuric acid were added within 25 minutes, and the reaction mixture was stirred for another 1 h at low temperature and 16 h at room temperature. Ice was added, the reaction mixture was adjusted to alkaline pH with 50% aqueous NaOH, and the aqueous phase was extracted twice with diethylether. The organic layers were combined, dried over magnesium sulfate, filtered and the solvent was evaporated under reduced pressure to yield 0.85 g of the desired product as a mixture of isomers and small amounts of the dinitro derivative which was used in the next reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642642B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-973bdd699fa14b72a522e13939755665 |
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| Source note | uspto-grants-2014_02 |
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