HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (S)-3-hydroxy-1-(4-methoxyphenethyl)pyrrolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | (S)-3-(4-Nitrobenzoyloxy)-1-(4-methoxyphenethyl)pyrrolidine | HCID 69901303 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (S)-3-hydroxy-1-(4-methoxyphenethyl)pyrrolidine | HCID 12148702 | — |
Reaction Steps
(S)-3-(4-Nitrobenzoyloxy)-1-(4-methoxyphenethyl)pyrrolidine (1.00 g, 2.70 mmol) was dissolved in methanol (20 ml), tetrahydrofuran (20 ml) and water (10 ml). 4 M-LiOH (3 ml) was added dropwise in the obtained solution, and they were stirred at room temperature for 1 hour. The solvent was evaporated under reduced pressure, and then the residue was distributed in water and ether. The organic layer was dried, and the solvent was evaporated under reduced pressure to obtain (S)-3-hydroxy-1-(4-methoxyphenethyl)pyrrolidine in the form of a light yellow oil (541 mg, 91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06528504B2 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-cfad9beb32ce42e68e3b879e7d04bdaa |
| Source note | uspto-grants-2003_03 |