HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (+/-)cis-1-(3-Phenylphenoxy)-2-methylaminoindane Hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | (+/-)cis-1-(3-Phenylphenoxy)-2-tert-butoxycarbonylaminoindane | HCID 18661288 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (+/-)cis-1-(3-Phenylphenoxy)-2-methylaminoindane Hydrochloride | HCID 18661287 | — |
Reaction Steps
To a solution of LiAlH4 (1.53 g, 40 mmol) in dry tetrahydrofuran (50 ml) under argon was added dropwise a solution of (±)cis-1-(3-phenylphenoxy)-2-tert-butoxycarbonylaminoindane (3.08 g, 8 mmol) in dry tetrahydrofuran (150 ml). The reaction was heated at reflux for 3 h then cooled with an ice/water bath and quenched with the minimum of water. The reaction was filtered and dried over MgSO4. Solvents were removed in vacuo and the residue subjected to column chromatography on silica gel eluting with 5% ethanol in chloroform to afford a colourless oil (1.38 g,) which was converted to the HCl salt and crystallised to afford the title compound as a white solid. m.p. >185° C. dec. (from methanol-diethyl ether).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05773463 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-a9c7b1e124b94d948c94e5e1099eac56 |
| Source note | uspto-grants-1998_06 |