Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324550Generated: October 30, 2026

Phenol → HCID 18621550, compound

https://huagongshe.com/reaction/324550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantTriethylamineHCID 8471—
Reactant1-Acetylpiperidine-4-carbonyl chlorideHCID 100950—
ReactantHCID 18621479HCID 18621479—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 18621550HCID 1862155080%

Reaction Conditions

Temperature25 °C

Reaction Steps

Phenyl N-acetylisonipecotate. To a suspension of N-acetylisonipecotoyl chloride (3.70 g, 19.50 mmol) in THF (60 mL) were added phenol (2.70 g, 27 mmol) and Et3N (5.0 mL, 36 mmol). The resulting heterogeneous mixture was stirred at 25° C. for 20 h, diluted with EtOAc (50 mL) and was washed with a saturated solution of NH4Cl (50 mL). The crude compound was purified by filtration on silica gel using EtOAc/n-hexane as eluant to afford the title compound as a colorless solid (3.45 g, 80%): mp 96-98 C; 1H NMR (CDCl3) d 1.60-1.95 (m, 2H), 2.00-2.2 (m, 5H), 2.70-3.00 (m, 2H), 3.10-3.30 (m, 1H), 3.75-3.90 (m, 1H), 4.40-4.60 (m, 1H), 7.06 (d, J=7.5 Hz, 2H), 7.22 (d, J=7.5 Hz, 1H), 7.38 (t, J=7.5 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06218404B1
Source datasetuspto-grants-2001_04
ORD IDord-149df84270b84f6dafd48acba05854e9
Source noteuspto-grants-2001_04