HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1498893Generated: October 27, 2026
Piperidine → Ethyl 3-nitro-4-(piperidin-1-yl)benzoate
https://huagongshe.com/reaction/1498893
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Ethyl 4-fluoro-3-nitrobenzoate | HCID 21277355 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 3-nitro-4-(piperidin-1-yl)benzoate | HCID 12493642 | 106.1% |
Reaction Steps
Ethyl 4-fluoro-3-nitrobenzoate (160 g, 0.752 mol) prepared in the Step 1-1-1 was suspended in ethanol (500 ml). Triethylamine (91.4 g, 0.903 mol) was added to the suspension, and under an ice cooling, piperidine (76.9 g, 0.903 mol) was slowly added thereto. After the mixture was stirred at a room temperature for 2 hours, a saturated sodium bicarbonate solution was added to the mixture, and the resulting mixture was subjected to extraction with ethyl acetate. The ethyl acetate layer was washed with a saturated sodium bicarbonate solution and a saturated saline solution in order, and then dried over anhydrous magnesium sulfate and concentrated. The concentrate was purified by silica gel column chromatography (n-hexane:ethyl acetate=4:1 to 3:1) to give the title compound (222 g, quantitative) as a poppy-red oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09200008B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-08aa21fb66624415afd2f8d3f01ffd81 |
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| Source note | uspto-grants-2015_12 |
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