HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Methanone, (2,4-difluorophenyl)-4-piperidinyl-, oxime, hydrochloride (1:1) | HCID 57357481 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazole | HCID 849421 | 81.1% |
Reaction Steps
A suspension of 11 g of 4-(2,4-difluoro-benzoyl)piperidine-oxime hydrochloride and 25 g of potassium hydroxide in 25 ml of water is heated to boiling with stirring for 2 hours. The reaction mixture is cooled to room temperature and extracted with toluene. The organic phase is dried over anhydrous sodium sulfate and evaporated in vacuo. The residual crude product is recrystallized from petroleum ether. Thus 7.1 g of the title compound are obtained. According to HPLC MS analysis the product contains 5% of 4-{6-[4′-(6′-fluoro-1′,2′-benzisoxazol-3′-yl)-piperidine-1′-yl]-1,2-benzisoxazol-3-yl}-piperidine, as a contamination (compound of the Formula VI).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07307168B2 |
| Source dataset | uspto-grants-2007_12 |
| ORD ID | ord-403354407f654bdea74d5597e06528d4 |
| Source note | uspto-grants-2007_12 |