HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → Ephedrine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | d-Ephedrine | HCID 9457 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ephedrine | HCID 9294 | — |
Reaction Steps
The hydroxy acid obtained above, 18.43 g. (0.093 mole) was dissolved in 200 ml. of ethyl acetate with gentle warming and to the solution was addeda solution of 15.04 g. (0.91 mole) of d-ephedrine, [α]578 =(+)11.4 (acetone), in 80 ml. ethyl acetate. The mixture was stirred at room temperature over night during which time a crop of crystals formed, was removed by filtration and air dried to obtain 18.3 g., M.P. 97°-99° C. This material was recrystallized by dissolving itin a minimum amount of hot ethyl acetate and allowing to stand at ambient temperature over night. After three such recrystallizations, 8.9 g. of thed-ephedrine salt of l-4-hydroxy-4-(p-fluorophenyl)butyric acid, M.P. 105.5°-106.5° C. was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04277404 |
| Source dataset | uspto-grants-1981_07 |
| ORD ID | ord-a1fc333e629b44b08d53984a6699367a |
| Source note | uspto-grants-1981_07 |