HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → N-Methyl-2-(p-tolyl)ethanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 2-(4-Methylphenyl)ethyl 4-methylbenzenesulfonate | HCID 285386 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-Methyl-2-(p-tolyl)ethanamine | HCID 22898654 | 180.8% |
Reaction Steps
9.2 g of methylamine are condensed at −20° C. into a solution of 5.8 g of 2-p-tolylethyl tosylate in 15 ml of abs. tetrahydrofuran and the mixture is stirred overnight at room temperature in a pressure vessel. After the pressure vessel has been opened at −20° C., it is allowed to come to room temperature in order to allow excess methylamine to evaporate. The reaction solution is taken up in ether, washed with water and saturated sodium chloride solution, dried over magnesium sulphate and concentrated to dryness in vacuo. 5.39 g of methyl-(2-p-tolylethyl)amine are obtained, which is reacted further as a crude product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06677324B1 |
| Source dataset | uspto-grants-2004_01 |
| ORD ID | ord-b35780ae1b2b434e9cd9b2a11ab538f2 |
| Source note | uspto-grants-2004_01 |