Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,4-Dinitrophenol | HCID 11348 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-(3-chloropropyl)piperidine hydrochloride | HCID 79624 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57637399 | HCID 57637399 | 102.3% |
Reaction Steps
To a stirred solution of 3,4-dinitrophenol (2 g, 10.9 mmol, 1 eq) in dimethyl formamide (40 ml), chloropropyl piperidine hydrochloride (2.8 g, 14.2 mmol, 1.3 eq) and potassium carbonate (3.2 g, 22.9 mmol, 2.1 eq) were added. The mixture was heated to 100° C. for 4 hours and the reaction was cooled to room temperature. The mixture was passed through a SCX column and eluted with 7N ammonia in methanol, the eluent was concentrated and the residue was subjected to chromatography on silica gel (100 g) to yield 1-[3-(3,4-dinitro-phenoxy)-propyl]-piperidine [3.45 g] as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07928231B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-93e04cf7649c43b6a22a0d541c299f78 |
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| Source note | uspto-grants-2011_04 |
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