Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl 4-fluoro-3-nitrobenzoateHCID 21277355—
SolventEthanolHCID 702—
ProductEthyl 3-nitro-4-(piperidin-1-yl)benzoateHCID 12493642106.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09200008B2
Source datasetuspto-grants-2015_12
ORD IDord-08aa21fb66624415afd2f8d3f01ffd81
Source noteuspto-grants-2015_12