HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → N-(2,4-Dimethoxybenzyl)prop-2-EN-1-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2,4-Dimethoxybenzylamine | HCID 597250 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(2,4-Dimethoxybenzyl)prop-2-EN-1-amine | HCID 4722371 | 40% |
Reaction Steps
0.32 ml of allylbromide (3.66 mM) and 0.7 ml of diisopropyl ethylamine (3.99 mM) were added to the reaction solution containing 500 mg of 2,4-dimethoxybenzylamine (3.33 mM) dissolved in methylene chloride with stirring and the solution was left alone at room temperature. After the reaction mixture was neutralized with 10% NaOH solution, the mixture was extracted with chloroform, washed with saturated NaCl solution, dried over MgSO4, filtered, and concentrated in vacuo. The resulting compound was purified with Silica gel column chromatography with a solvent mixture mixed with methanol and chloroform (1:9) as an eluant to give 276 mg of allyl-(2,4-dimethoxybenzyl)amine (1b) (yield: 40%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07723376B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-6b215f6b73874ee59a4ddeccff7e215c |
| Source note | uspto-grants-2010_05 |