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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43339Generated: October 24, 2026

Acetic Acid → tert-Butyl 4-(3-fluoroanilino)piperidine-1-carboxylate

https://huagongshe.com/en/reaction/43339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant3-FluoroanilineHCID 9742—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Solvent1,2-DichloroethaneHCID 11—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 4-(3-fluoroanilino)piperidine-1-carboxylateHCID 2313759182%

Reaction Steps

A solution of 1,1-dimethylethyl 4-oxo-1-piperidinecarboxylate (1.91 g, 9.53 mmol), 3-fluoroaniline (1.06, 9.53 mmol) and acetic acid (0.55 ml, 9.53 mmol) in 1,2-DCE (50 ml) was stirred at room temperature overnight. Sodium tri(acetoxy)borohydride (2.82 g, 13.3 mmol) was then added, stirred for 8 hrs and then allowed to stand at room temperature. The reaction mixture was diluted with DCM and washed with NaHCO3 solution, dried over MgSO4 and then concentrated to give the product which was purified by column chromatography. Elution with 0-40% EtOAc/pentane gave the title compound as a white solid (2.3 g). δH (CDCl3, 250 MHz) 7.08 (1H, q), 6.35 (3H, m), 4.04 (1H, br s), 3.65 (1H, br s), 3.38 (1H, m), 2.92 (2H, m), 2.02 (2H, m), 1.47 (9H, s), 1.34 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536182B2
Source datasetuspto-grants-2013_09
ORD IDord-ed5e4844a6594da5b9d1c7dabd6a94e7
Source noteuspto-grants-2013_09