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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583042Generated: November 3, 2026

N-Benzylphenethylamine → HCID 22716818, compound

https://huagongshe.com/reaction/1583042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-BenzylphenethylamineHCID 65055—
ReactantDiisopropylethylamineHCID 81531—
Reactant[2-(Benzyloxy)-5-formylphenyl]methyl methanesulfonateHCID 21957468—
SolventDimethylformamideHCID 6228—
ProductHCID 22716818HCID 2271681887%

Reaction Steps

To a solution of N-benzyl-N-(2-phenylethyl)amine (351 mg) and diisopropyl-ethylamine (145 mg) in dimethylformamide (1.5 ml) was added 3-[[(methylsulfonyl)oxy]methyl]-4-phenylmethoxybenzaldehyde (355 mg). After stirring at room temperature for 3 hours, the reaction mixture was partially concentrated under reduced pressure and the residue was purified by flash chromatography column using petroleum ether:diethyl ether (1:3) as eluant. The pure fractions were combined and evaporated under reduced pressure to give 4-phenylmethoxy-3-[[N-phenylmethyl-N-(2-phenylethyl)amino]methyl]benzaldehyde (420 mg) as a gum. 1H NMR (CDCl3) δ9.89 (s, 1H, CHO); 5.20 (s, 2H); 3.88 (s, 2H); 3.85 (s, 2H); 2.92 (m, 4H, CH2CH2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06740670B2
Source datasetuspto-grants-2004_05
ORD IDord-d93e98fb43ab4ddeadcbf9f58ed91ebf
Source noteuspto-grants-2004_05