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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2087213Generated: October 27, 2026

Water → Tert-butyl 4-[3-(propionylamino)phenyl]-1-piperidinecarboxylate

https://huagongshe.com/reaction/2087213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPropionyl chlorideHCID 62324—
Reactanttert-Butyl 4-(3-aminophenyl)piperidine-1-carboxylateHCID 22049268—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-[3-(propionylamino)phenyl]-1-piperidinecarboxylateHCID 22049473104.1%

Reaction Steps

Propionyl chloride (5.53 g, 0.0597 mol) was added dropwise to a solution of tert-butyl 4-(3-aminophenyl)-1-piperidinecarboxylate (15.0 g, 0.0543 mol) and TEA (16.5 g, 0.163 mol) in THF (200 mL) and the mixture was stirred at room temperature for 3 h. Water (50 mL) was added to the reaction mixture, the aqueous layer was extracted with CH2Cl2 (3×100 mL), and the combined organic extracts were washed with brine (50 mL), dried over Na2SO4 and concentrated under reduced pressure. The residue was purified by chromatography on silica using hexane/EtOAc (10:1) to afford the product (18.8 g, 99%). 1H NMR (400 MHz, CDCl3) δ 7.48 (s, 1H), 7.34-7.21 (m, 3H), 6.93 (d, 1H, J=7.4 Hz), 2.77 (t, 2H, J=11.5 Hz), 2.68-2.58 (m, 1H), 2.38 (q, 2H, J=7.6 Hz), 1.87-1.67 (m, 4H), 1.67-1.54 (m, 2H), 1.48 (s, 9H), 1.25 (t, 3H, J=7.5 Hz); ESMS m/e: 333.4 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06727264B1
Source datasetuspto-grants-2004_04
ORD IDord-5234561dd3b34ea8bd717b763e575e2b
Source noteuspto-grants-2004_04