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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109617Generated: November 1, 2026

(4-Aminophenoxy)benzene → HCID 4548294, compound

https://huagongshe.com/reaction/2109617

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Aminophenoxy)benzeneHCID 8764—
ReactantEthyl AcetateHCID 8857—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Chloronicotinoyl chlorideHCID 2774541—
SolventDichloromethaneHCID 6344—
ProductHCID 4548294HCID 4548294—

Reaction Steps

2-Chloronicotinoyl chloride (9.15 g, 0.052 mol) was added to a stirred solution of 4-phenoxyaniline (10.00 g, 0.054 mol) and DIEA (10.00 ml, 0.057 mol) in CH2Cl2 (100 ml) at RT. The mixture stirred for 48 h before removal of solvent under reduced pressure. The resulting residue was dissolved EtOAc and washed several times with saturated NaHCO3 aqueous solution and brine, respectively. The organic layer was dried over Na2SO4 and evaporated to leave a solid. This material was re-crystallized from EtOAc/Hexane mixture, followed by filtration and rinsing with Et2O to leave the desired compound as a white solid. MS m/z: 325 (M+1); 323 (M−1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514564B2
Source datasetuspto-grants-2009_04
ORD IDord-1eeeff5f9d7d46b6a23b31b5a0f6b96c
Source noteuspto-grants-2009_04