Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419363Generated: October 31, 2026

Acetic Acid → 1,1-Dimethylethyl 4-[4-(2-fluoroethyl)-1-piperazinyl]-1-piperidinecarboxylate

https://huagongshe.com/reaction/419363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant1-(2-Fluoroethyl)piperazine dihydrochlorideHCID 66545688—
Solvent1,2-DichloroethaneHCID 11—
Product1,1-Dimethylethyl 4-[4-(2-fluoroethyl)-1-piperazinyl]-1-piperidinecarboxylateHCID 5945268894.6%

Reaction Steps

1,1-Dimethylethyl 4-oxo-1-piperidinecarboxylate (38.9 g, 195 mmol) and 1-(2-fluoroethyl)piperazine dihydrochloride (20 g, 97 mmol) were dissolved in 485 mL 1,2-DCE. TEA (81.5 mL, 585 mmol) was added and the reaction was stirred for 30 min. HOAc (8.4 mL, 146 mmol) was added and the reaction was stirred for an additional 30 min followed by the addition of sodium triacetoxyborohydride (49.6 g, 234 mmol). The reaction was stirred overnight. Saturated aqueous NaHCO3 solution was added carefully until the reaction stopped bubbling. Aqueous layer was then extracted with DCM (1×) and EtOAc (3×). Combined organic layers were dried over MgSO4, filtered and concentrated in vacuo. The resulting crude product was absorbed onto silica gel and purified by flash chromatography to give title compound of step C (28.95 g, 94%). 1H NMR (400 MHz, DMSO-d6) δ ppm 4.39-4.57 (m, 2H), 3.90 (d, J=12.46 Hz, 2H), 2.61-2.73 (m, 2H), 2.47-2.61 (m, 2H), 2.36-2.47 (m, 8H), 2.24-2.35 (m, 1H), 1.69 (d, J=12.46 Hz, 2H), 1.37 (s, 9H), 1.14-1.26 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093239B2
Source datasetuspto-grants-2012_01
ORD IDord-6b61fea9dace4bc697635b5b9d2ba3aa
Source noteuspto-grants-2012_01