HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → Methyl(3-phenoxypropyl)amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Benzene, (3-bromopropoxy)- | HCID 68522 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl(3-phenoxypropyl)amine | HCID 22067856 | — |
Reaction Steps
3.57 g of methylamine is condensed in a solution of 1.6 ml of 3-phenoxy-propylbromide 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. 2.01 g of methyl-(3-phenoxy-propyl)-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-fc7b3c344a2b4cff8abb4059c487e8b0 |
| Source note | uspto-grants-2004_08 |