HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 2-Amino-7-hydroxytetralin hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 7-Methoxy-1,2,3,4-tetrahydronaphthalen-2-amine hydrochloride | HCID 14750915 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 2-Amino-7-hydroxytetralin hydrobromide | HCID 14750916 | — |
Reaction Steps
A suspension of the compound obtained in step (b) (6.6 g) in 48% hydrobromic acid (80 ml) is refluxed for 2 hours. The obtained solution is evaporated to dryness and the residue is twice taken up in absolute ethanol and concentrated to dryness. An oily product is thus obtained which is dissolved in hot isopropanol (20 ml). Ethyl ether (30 ml) is added thereto and a crystalline precipitate of 2-amino-7-hydroxytetralin hydrobromide (6.8 g) is obtained. M.p. 171°-173° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05312961 |
| Source dataset | uspto-grants-1994_05 |
| ORD ID | ord-18bf23df7b564c1e8c7fed68f48f933e |
| Source note | uspto-grants-1994_05 |