HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminotetralin → N-(1,2,3,4-tetrahydronaphth-2-yl)-2-hydroxy-3-(2-naphthyloxy)propanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminotetralin | HCID 34677 | — |
| Reactant | 2-Naphthyl glycidyl ether | HCID 92995 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(1,2,3,4-tetrahydronaphth-2-yl)-2-hydroxy-3-(2-naphthyloxy)propanamine | HCID 19788252 | 53.2% |
Reaction Steps
A mixture of 1-(2-naphthyloxy)-2,3-epoxypropane (1.95 g), 2-aminotetralin (2.65 g) and ethanol (35 ml) is heated to the reflux temperature for 5 hours. The solvent is then evaporated off and the thus obtained solid residue is crystallized from ethyl acetate (5 ml), recovered by filtration, washed with ethyl acetate and then with ethyl ether, and dried yielding 1.8 g of N-(1,2,3,4-tetrahydronaphth-2-yl)-2-hydroxy-3-(2-naphthyloxy)propanamine, as the free base; m.p. 102°-115° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05254595 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-6d61e845ef5d45ed9a722e30b04140de |
| Source note | uspto-grants-1993_10 |