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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117637Generated: October 31, 2026

Nitric Acid → 4-(4-Nitrophenyl)piperidine

https://huagongshe.com/reaction/2117637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantSulfuric AcidHCID 1118—
ReactantSodium HydroxideHCID 14798—
Reactant4-PhenylpiperidineHCID 69873—
ReactantSodium BicarbonateHCID 516892—
SolventAcetic AcidHCID 176—
Product4-(4-Nitrophenyl)piperidineHCID 15925817—

Reaction Conditions

Temperature25 °C

Reaction Steps

4-Phenylpiperidine (8 g, 49 mmol) was dissolved in 40 mL acetic acid and stirred with cooling below 25° C. while adding a solution of 2.64 mL sulphuric acid in 40 mL acetic acid. The solution was stirred at 20° C. while adding a solution of 2.08 mL 99% nitric acid in 20 mL acetic acid. Sulphuric acid (40 mL) was added without cooling, the temperature peaking at 58° C. When the solution had cooled to 25° C. it was added to 100 g ice/water and basified with a total of 150 g sodium hydrogen carbonate at 40° C. The mixture was then brought to pH 14 with 5M-sodium hydroxide solution. The mixture was extracted with dichloromethane (3×150 mL), dried with sodium sulphate and evaporated giving a pale yellow solid. Recrystallisation from a total of 180 mL cyclohexane (hot filtration) gave the product as pale beige solid. NMR δ 8.18(d,2H), 7.40(d,2H), 3.21(m,2H), 2.77(m,3H), 1.82(m,3H), 1.68(m,2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442698B2
Source datasetuspto-grants-2008_10
ORD IDord-ee271dfb7b754cd991b3672af842bdb6
Source noteuspto-grants-2008_10