HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Benzylphenethylamine → HCID 22716818, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Benzylphenethylamine | HCID 65055 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | [2-(Benzyloxy)-5-formylphenyl]methyl methanesulfonate | HCID 21957468 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22716818 | HCID 22716818 | 87% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06740670B2 |
| Source dataset | uspto-grants-2004_05 |
| ORD ID | ord-d93e98fb43ab4ddeadcbf9f58ed91ebf |
| Source note | uspto-grants-2004_05 |