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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014194Generated: November 1, 2026

Potassium Carbonate → 1-(4-Amino-3-methoxyphenyl)piperidin-4-ol

https://huagongshe.com/reaction/1014194

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPiperidin-4-olHCID 79341—
Reactant5-Fluoro-2-nitroanisoleHCID 2779250—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product1-(4-Amino-3-methoxyphenyl)piperidin-4-olHCID 5735346063%

Reaction Steps

A solution of 4-fluoro-2-(methyloxy)-1-nitrobenzene (3.0 g, 17.5 mmol), 4-hydroxypiperidine (1.77 g, 17.5 mmol) and potassium carbonate (2.9 g, 21 mmol) in DMSO was stirred for 24 h. The reaction was diluted with water and extracted three times with Ethyl acetate. The combined organic solutions were dried over MgSO4 and concentrated. The resulting residue was stirred in ethanol and acetic acid with 10% Pd/C under 30 psi of hydrogen for 16 hr. The reaction was filtered through a pad of celite, rinsed with Ethyl acetate. The filtrate was concentrated and dissolved in methylene chloride. The organic solution was washed with saturated sodium bicarbonate, dried over MgSO4, and concentrated to give 1-[4-amino-3-(methyloxy)phenyl]-4-piperidinol (2.44 g, 63% yield over 2 steps). 1H NMR (400 MHz, d6-DMSO) δ 6.49-6.45 (m, 2H), 6.27 (dd, J=8.4 and 2.4 Hz, 1H), 4.60 (d, J=4.0 Hz, 1 H), 4.18 (s, 2H), 3.71 (s, 3H), 3.54-3.48 (m, 1H), 3.25-3.22 (m, 2H), 2.63-2.56 (M, 2H), 1.80-1.76 (m, 2H), 1.51-1.42 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981903B2
Source datasetuspto-grants-2011_07
ORD IDord-b33ef526b01d4d2686d331f438668f1b
Source noteuspto-grants-2011_07