HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → Serinol ketoprofen Hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Hydrogen chloride-ethyl acetate | HCID 21866389 | — |
| Reactant | Boc-serinol ketoprofen | HCID 86623045 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Serinol ketoprofen Hydrochloride | HCID 86623046 | — |
Reaction Steps
Boc-serinol-ketoprofen (0.428 mmol) was dissolved in dichloromethane (1 ml), and 4 N hydrochloric acid/ethyl acetate (4 ml) was added thereto under ice-cooling, followed by stirring for 2 hours while gradually returning to room temperature. After confirming disappearance of Boc-serinol-ketoprofen by TLC, diethyl ether and hexane were added thereto, and the resulting precipitate was centrifuged. The thus obtained precipitate was dried under reduced pressure to give the titled compound (243.6 mg, qu.). The structure was identified by 1H-NMR (CDCl3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07879817B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-eaa01563653c436caeac4284f6056bf6 |
| Source note | uspto-grants-2011_02 |