HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 2-(2-Methoxyphenyl)-N-methylethan-1-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 14687316 | HCID 14687316 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(2-Methoxyphenyl)-N-methylethan-1-amine | HCID 13092505 | 87% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To N-(t-Butyloxycarbonyl)-2-(2-methoxyphenyl)-ethylamine (182.7 mmol, 45.9 g) in dry tetrahydrofuran (200 mL) at 0° C. was added, in portions, lithium aluminum hydride (219.2 mmol, 8.3 g) under N2. After stirring at 0° C. for 1 hour, the ice-bath was removed and then the reaction heated to reflux for 24 hours, cooled to room temperature then to 0° C.; the excess lithium aluminum hydride was destroyed very carefully with 20% potassium hydroxide solution (1.3 equivalent). After removing the salt by filtration, the filtrate was dried then evaporated to dryness to give product as a white solid (26.2 g, 87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05922697 |
| Source dataset | uspto-grants-1999_07 |
| ORD ID | ord-7bdd198fd2c54cdbbacc8d539aa6f59a |
| Source note | uspto-grants-1999_07 |