HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropylamine → Levopropranolol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropylamine | HCID 6363 | — |
| Reactant | (2S)-2-((1-Naphthalenyloxy)methyl)oxirane | HCID 148933 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Levopropranolol | HCID 91536 | 92.6% |
Reaction Steps
A solution of (S)-(+)-glycidyl naphthyl ether (20 g, 0.1 m) and isopropylamine (10 g, 0.17 m) in methanol (100 mL) was refluxed for 1 hour and evaporated to dryness. The residue was taken up with ether (200 mL), washed with water and dried over MgSO4. After filtering, the filtrate was acidified with gaseous HCl. The crude solid was recrystallized from ethanol to afford 24 g (81%) of pure 1-propranolol, mp 198°-200° C., [α]D25 -26.8 (c 1, EtOH). NMR and IR were consistent with the assigned structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04990668 |
| Source dataset | uspto-grants-1991_02 |
| ORD ID | ord-09f86e121b944fc3b6e0dad1e3b70f51 |
| Source note | uspto-grants-1991_02 |