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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1832220Generated: October 27, 2026

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

https://huagongshe.com/reaction/1832220

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 numberUS07067534B1
Source datasetuspto-grants-2006_06
ORD IDord-421dc3d39e8b40e69b90906c1289b02c
Source noteuspto-grants-2006_06