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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920552Generated: October 26, 2026

4-Benzyl-2-(4-bromo-phenyl)-morpholine → 4-Benzyl-2-[4-(2,6-dichloro-benzyl)-phenyl]-morpholine

https://huagongshe.com/reaction/920552

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Benzyl-2-(4-bromo-phenyl)-morpholineHCID 58097879—
ReactantHCID 178478101HCID 178478101—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
Product4-Benzyl-2-[4-(2,6-dichloro-benzyl)-phenyl]-morpholineHCID 6703258894%

Reaction Steps

To a mixture of 2,6-dichlorobenzylzinc chloride (7.95 mL; 0.50 mol/l in THF; 3.97 mmol) and tetrakis(triphenylphosphine)palladium(0) (83.48 mg; 0.07 mmol) in THF (25 mL) was added 4-benzyl-6-(4-bromo-phenyl)-morpholine (1.20 g; 3.61 mmol). The resulting mixture was stirred at RT for 2 hours, and subsequently heated under reflux, for 2 h. After cooling to RT the mixture was concentrated in vacuo. The residue was partitioned between 5% aqueous NaHCO3 and EtOAc. The organic layer was dried (Na2SO4), filtered, and concentrated in vacuo. The residue was purified by column chromatography (SiO2, Et2O:hexanes 1:1) to afford 4-benzyl-2-[4-(2,6-dichloro-benzyl)-phenyl]-morpholine (1.40 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273017B2
Source datasetuspto-grants-2016_03
ORD IDord-634a07f6e2df4df185150c5cfd33bcc7
Source noteuspto-grants-2016_03