HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428968Generated: October 30, 2026
1-Hexylpyrrole-2,5-dione → 3-Hexyl-6-(3-nitrophenyl)-6-(2,2,2-trifluoroethyl)-3-azabicyclo[3.1.0]hexane-2,4-dione
https://huagongshe.com/reaction/428968
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Hexylpyrrole-2,5-dione | HCID 464134 | — |
| Reactant | 3,3,3-Trifluoro-1-(3-nitrophenyl)-1-propanone hydrazone | HCID 73698598 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-Hexyl-6-(3-nitrophenyl)-6-(2,2,2-trifluoroethyl)-3-azabicyclo[3.1.0]hexane-2,4-dione | HCID 22141283 | 223.4% |
Reaction Steps
3,3,3-Trifluoro-1-(3-nitrophenyl)-1-propanone hydrazone (Preparation 104, 150 mg, 0.6 mmol) was dissolved in dioxan (10 ml) and manganese dioxide (600mg, 7.1 mmol) was added in one portion at room temperature. After stirring for 30 min, the reaction mixture was filtered through a pad of ArbocelTm directly into a flask containing a stirred solution of 1-hexyl-1H-pyrrole-2,5-dione (Preparation 56, 44 mg, 0.2 mmol) in dioxan (10 ml). The filter pad was washed further with dioxan (40 ml), and was also added to the reaction mixture. The resulting amber-yellow solution was stirred for 16 h at room temperature. The colourless mixture was then heated under reflux for 1 h before cooling to room temperature and concentrating in vacuo. The residue was purified by chromatography on silica gel (10 g), eluting with hexane:ether (2:1) to give the product as a white solid (178 mg, 74%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06313312B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-a0aca4ed46414e409b9861f1f4efc3b1 |
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| Source note | uspto-grants-2001_11 |
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