HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 70457521, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 20225230 | HCID 20225230 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 70457521 | HCID 70457521 | — |
Reaction Steps
N-[2-(4-Carbomethoxymethoxyphenyl)-1-methylethyl]-2-methoxy-2-phenylethanamine (3.09 g) in dry tetrahydrofuran (30 ml) was added dropwise, with stirring, to a suspension of lithium aluminium hydride (1.65 g) in dry tetrahydrofuran (40 ml) and the resultant mixture heated under reflux for five hours. After cooling, water (1.7 ml), 10% aqueous sodium hydroxide (1.7 ml) and water (3.4 ml) were added carefully. Filtration and evaporation of the filtrate to dryness gave an oil which was converted to its hydrochloride salt by addition of ethereal hydrogen chloride. Crystallisation from methanol-ethyl acetate gave the title compound, mp 100°-2° C., as a 90:10 mixture of diastereoisomers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04629737 |
| Source dataset | uspto-grants-1986_12 |
| ORD ID | ord-4de354315513481a8cf9bcb9d82d2b3c |
| Source note | uspto-grants-1986_12 |