HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → 3-(benzyloxy)-N-methylpropan-1-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Benzyl 3-Bromopropyl Ether | HCID 2776064 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(benzyloxy)-N-methylpropan-1-amine | HCID 23497039 | — |
Reaction Steps
3.57 g of methylamine is condensed in a solution of 1.8 ml of (3-bromo-propoxymethyl)-benzene in 15 ml of anhydrous tetrahydrofuran at −78° C., and it is stirred overnight at room temperature in a pressurized reactor. After the pressurized reactor was opened at −20° C., it is allowed to come to room temperature to allow excess methylamine to evaporate off. Then, the reaction solution is added to saturated sodium chloride solution, extracted with ether, dried on magnesium sulfate and concentrated by evaporation in a vacuum. 1.91 g of (3-benzyloxy-propyl)-methyl-amine is obtained as a crude product, which is used without further purification in the next stage.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06780855B2 |
| Source dataset | uspto-grants-2004_08 |
| ORD ID | ord-0fbd7af9fbb546fe9f252085efa052d8 |
| Source note | uspto-grants-2004_08 |