HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → Salbutamol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Levalbuterol Hydrochloride | HCID 123601 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Salbutamol | HCID 2083 | — |
| Product | Levalbuterol Hydrochloride | HCID 123601 | — |
Reaction Steps
In a 2 L reactor equipped with a condenser, thermometer, and mechanical stirrer at 20° C. and under nitrogen, a suspension of wet levalbuterol hydrochloride (97.6 g), ethylacetate (440 mL) and methanol (49 mL) was formed. The suspension was stirred at 22° C.±2° C. for 4 hours. The solid was collected by filtration and washed with an ethylacetate:methanol mixture (90:10, 97 mL), and ethylacetate (2×97 mL). The product was dried at 22° C.±2° C. under vacuum (res. press. 40-45 mm Hg) for 24 hours to obtain 64.0 g (dry weight) in 92.5% yield from pure (R)-SLB.D-DBTA. The overall yield from racemic salbutamol to pure levalbuterol hydrochloride: 39.5%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07482489B2 |
| Source dataset | uspto-grants-2009_01 |
| ORD ID | ord-34339f2b01244dfa8365eb04a1c578d4 |
| Source note | uspto-grants-2009_01 |