HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → N-benzyl-1-(3,4-dimethoxyphenyl)ethanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | 1-(3,4-Dimethoxyphenyl)ethan-1-amine | HCID 3159243 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Catalyst | Pyridine | HCID 1049 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-benzyl-1-(3,4-dimethoxyphenyl)ethanamine | HCID 2756621 | 100% |
Reaction Steps
A mixture containing 18.1 g of 1-amino-1-(3,4-dimethoxyphenyl)-ethane (J. Chem. Soc. 1963, 4289), 10,6 g of benzaldehyde and 1 drop of pyridine in 100 ml of methanol is let stand at 20° C. for 2 days, then 3.8 g of sodium borohydride are added during 30 minutes and stirred for additional 3 hours. After evaporation of the solvent, the residue is diluted with water, extracted with chloroform, the organic phase is dried and evaporated to give 27.1 g of the crude title compound, which can directly be used in the process described in Example 6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04988730 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-410bde7194ba4142b2429f990e3a0d04 |
| Source note | uspto-grants-1991_01 |