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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416177Generated: November 3, 2026

Acetic Acid → N-benzyl-1-phenylethylamine

https://huagongshe.com/reaction/2416177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantN-benzyl-1-phenylethanimineHCID 297338—
ReactantHCID 57230745HCID 57230745—
ReactantHCID 178418361HCID 178418361—
CatalystTetrabutylammonium IodideHCID 67553—
SolventTolueneHCID 1140—
ProductN-benzyl-1-phenylethylamineHCID 519427—

Reaction Steps

The process is carried out as in Example 6, but the reaction conditions are modified as follows: 0.636 g (3 mmol) of N-benzyl-N-(1-phenylethylidene)amine, 10.2 mg (0.0152 mmol) of [Ir(1,5-cyclooctadiene)Cl]2, 21.4 mg (0.0333 mmol) of {(R)-1-[(S)-2-diphenylphosphino)ferrocenyl]}ethyl-di(3,5-dimethylphenyl)phosphine (ligand) and 15 mg (0.04 mmol) of tetrabutylammonium iodide, 2 ml of acetic acid, 15 ml of toluene, 30 bar of hydrogen, reaction temperature: 25° C. The reaction time is 20 minutes. The conversion is complete, the ee 31%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06822118B1
Source datasetuspto-grants-2004_11
ORD IDord-2ca8f37cc2294b07b0de46e71d579a36
Source noteuspto-grants-2004_11