HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Tartrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | L-Tartaric acid | HCID 444305 | — |
| Reactant | trans-(-)-4-(4-Fluorophenyl)-3-hydroxymethylpiperidine monohydrate | HCID 69039254 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | Tartrate | HCID 119400 | 35.5% |
| Product | (3S,4R)-4-(4-Fluorophenyl)-3-piperidinemethanol | HCID 9855829 | 35.5% |
Reaction Steps
Subsequently, 10.00 g (44.0 mmol) of the trans-(−)-4-(4-fluorophenyl)-3-hydroxymethylpiperidine monohydrate, 6.60 g (44.0 mmol) of L-tartaric acid, and 50 ml of methanol were mixed together, and 50 ml of isopropanol was added to the resulting mixture under ice-cooling. The mixture was allowed to stand to precipitate crystals, and the resulting crystals were filtered. The crystals were washed with a 10 ml mixed solvent of 5 ml of methanol and 5 ml of isopropanol and dried, to give 5.60 g (15.6 mmol) of L-tartrate of trans-(−)-4-(4-fluorophenyl)-3-hydroxymethylpiperidine (yield: 35.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06316628B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-b163e41d8342420fa36e29a1adce8e7a |
| Source note | uspto-grants-2001_11 |