HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → N-Methylhomoveratrylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | HCID 4128531 | HCID 4128531 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-Methylhomoveratrylamine | HCID 77039 | — |
Reaction Steps
The product of (i) was reduced in dry tetrahydrofuran or diethylether in conventional manner by the addition of 3 equivalents of LiAlH4 and subsequent refluxing of the mixture for 0.5-1 hr. After cooling and filtration, the solvent was evaporated and the product obtained by first extraction of the ethereal phase at pH 4, then at pH 10 with methylene chloride. Drying and evaporation of the solvent yielded 50-60% nearly pure oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05494933 |
| Source dataset | uspto-grants-1996_02 |
| ORD ID | ord-bd266cbdf6bb41e0b400ff2f40e7548b |
| Source note | uspto-grants-1996_02 |