HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1-Aminomethyl-5-acetoxy-3-phenyl-3,4dihydronaphthalene hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-Aminomethyl-5-hydroxy-3-phenyl-3,4-dihydronaphthalene | HCID 20069041 | — |
| Reactant | 1-Aminomethyl-5-hydroxy-3-phenyl-3,4-dihydronaphthalene formic acid salt | HCID 20069043 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | 1-Aminomethyl-5-acetoxy-3-phenyl-3,4dihydronaphthalene hydrochloride | HCID 20069070 | — |
Reaction Steps
A suspension of 1-aminomethyl-5-hydroxy-3-phenyl-3,4-dihydronaphthalene formic acid salt, the product of Example 2, in acetic anhydride saturated with anhydrous hydrogen chloride is stirred at ambient temperature for 48 h. A solid is collected by filtration and washed with diethyl ether. Crystallization of the crude material is achieved by dissolving the powder in hot ethanol, adding water, filtering the solution hot and allowing it to cool. Filtration and drying of the solid collected affords 1-aminomethyl-5-acetoxy-3-phenyl-3,4dihydronaphthalene hydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04994486 |
| Source dataset | uspto-grants-1991_02 |
| ORD ID | ord-7146eb8919b24b5283fe3bd2333e53fd |
| Source note | uspto-grants-1991_02 |